Source: FDA, document on file. FDA released the Form 483 itself. The document linked above is our copy of FDA's file, stored by us so the link cannot break, and FDA's own copy is linked beside it. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 2410662.
Observations6
Issue DateJuly 24, 2015
StatusNo Warning Letter
Establishment TypeManufacturer
Related Inspections7
Establishment Details
Firm
Wyeth Pharmaceutical Division of Wyeth Holdings LLC
Issued To
Wyeth Pharmaceutical,Div Wyeth Holding Corp
Location
Pearl River, New York, United States
FEI Number
2410662
Establishment Type
Manufacturer
Product Type
Drugs
Issue Date
July 24, 2015
Country
United States
Inspection History, 2008 to 2025
NAI2
VAI5
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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