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Peerless Injection Molding Hit for Complaint Handling

June 17, 2020

The FDA has cited Peerless Injection Molding for lax handling of product complaints at its Garden Grove, Calif., plant.

An FDA inspection of the facility found that some complaints about problems with heat-sealed dentistry products had incorrect dates and lacked documentation on the corrective actions taken.

Not all complaints were assessed to determine whether medical device reports should be filed with the FDA, according to the Form 483 inspection report.

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