We use cookies to provide you with a better experience. By continuing to browse the site you are agreeing to our use of cookies in accordance with our Cookie Policy.
Accept
  • SKIP TO CONTENT
  • SKIP NAVIGATION
  • Drug & Device Products
    • FDAnews Books Library
    • Events
    • Form 483s Database
    • Publications
    • Webinar Training Pass
    • eCFR and Guidances
    • Books
  • Clinical Products
  • Advertising
  • White Papers
  • Contact Us
  • About Us
  • COVID-19
  • Sign In
  • Create Account
  • Sign Out
  • My Account
Home » Form 483

With a subscription to our Form 483s Database, you get instant, unlimited access to more than 8,600 Form 483s. They’re literally just a click away. Choose from the list of most recently added 483s below or use the multi-function search engine to the right. Once you’ve found the 483s you want, just hit the Download button and they’re all yours. Nonmembers have the option to either subscribe on the spot or purchase their 483s individually.

We FOIA ALL Form 483s issued every month. If when you search you don't find what you're looking for, simply give us a call 703.538.7600 and we'll do our best to get it for you.

FOIAing is not an exact science with promised deadlines of delivery. We will do all we can to get you the information you need.

LOGIN

Buy One Year Single-User Unlimited Access for $1,297

Also available: Take advantage of our multi-user and site licenses of the Form 483s Database so you’ll have the most-informed workforce! Contact Will Tuttle, Business Development Representative at wtuttle@fdanews.com or +1 612.216.2948 to receive a custom quote.


Search by date, by keyword, by category (drug, device or clinical), by investigator name or by a region. 

If you don't see a Form 483 that you're looking for, please give us a call on 703.538.7600 or email customer service and we'll do our best to get it for you.

FOIAing is not an exact science, we FOIA ALL Form 483s issued but they can take time to come to us, especially if from an international inspection.

No Cover Available

iScience Interventional

Issue Date

Aug 16, 2010

Category

Device

Region

Pacific
Investigator(s): Lydia S. Chan
Download
No Cover Available

Howmedica Osteonics Corp.

Issue Date

Aug 12, 2010

Category

Device

Region

Central
Investigator(s): Robert G. Ruff
Download
No Cover Available

Abbott Point of Care, Inc.

Issue Date

Aug 11, 2010

Category

Device

Region

Central
Investigator(s): Kinh Q. Mac
Download
No Cover Available

Align Technology, Inc.

Issue Date

Aug 09, 2010

Category

Device

Region

Pacific
Investigator(s): Linda Linh T. Nguyen
Download
No Cover Available

Hitachi Chemical Diagnostics, Inc.

Issue Date

Aug 06, 2010

Category

Device

Region

Pacific
Investigator(s): Jeffrey W. Shrifter
Download
No Cover Available

Hospira, Inc.

Issue Date

Jul 28, 2010

Category

Device

Region

Pacific
Investigator(s): Timothy C. Grome
Download
No Cover Available

Marlen Manufacturing & Development Co.

Issue Date

Jul 27, 2010

Category

Device

Region

Central
Investigator(s): Benjamin J. Dastoli
Download
No Cover Available

Dream Systems, LLC

Issue Date

Jul 27, 2010

Category

Device

Region

Pacific
Investigator(s): Lydia S. Chan
Download
No Cover Available

Cerv-I-Trac

Issue Date

Jul 26, 2010

Category

Device

Region

Central
Investigator(s): Melissa J. Ireland
Download
No Cover Available

Abbott Molecular

Issue Date

Jul 23, 2010

Category

Device

Region

Central
Investigator(s): Jesse A. Vazquez
Download
No Cover Available

American I.V. Products, Inc.

Issue Date

Jul 21, 2010

Category

Device

Region

Central
Investigator(s): James W. Leonette
Download
No Cover Available

Replication Medical, Inc.

Issue Date

Jul 21, 2010

Category

Device

Region

Central
Investigator(s): Amy M. Cramer
Download
Previous 1 2 … 811 812 813 814 815 816 817 818 819 Next

Search By Date Issued

Search By Category

Drug
Device
Clinical

Search By Company/

Clinical Investigator

Search By Region

Search By FDA Investigator

Search By Keyword

  • Drug Products
    • Quality
    • Regulatory Affairs
    • GMPs
    • Inspections and Audits
    • Postmarket Safety
    • Submissions and Approvals
    • Research and Development
    • Commercial Operations
  • Device Products
    • Quality
    • Regulatory Affairs
    • QSR
    • Inspections and Audits
    • Postmarket Safety
    • Submissions and Approvals
    • Research and Development
    • Commercial Operations
  • Clinical Products
    • Trial Design
    • Data Integrity
    • GCP
    • Inspections and Audits
    • Transparency
  • Privacy Policy
  • Do Not Sell or Share My Data
Footer Logo

300 N. Washington St., Suite 200, Falls Church, VA 22046, USA

Phone 703.538.7600 – Toll free 888.838.5578

Copyright © 2023. All Rights Reserved. Design, CMS, Hosting & Web Development :: ePublishing