Issued: 9/19/10
Region: Northeast
Category: Device 483s
Inspection date range: 8/24/11-9/19/11
Pages: 2
Company: Haemonetics Corp.
400 Wood Rd.
Braintree, MA 02184-2412
Inspector(s): Sandra P. White
Observations: Summary recall status document reviewed showed no periodic (monthly) status reports were submitted per FDA district office instructions.
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