Source: FDA record for this establishment. FDA publishes inspections or enforcement actions for this establishment, listed further down this page, but we have not matched this particular Form 483 to a document or an inspection date FDA has released. It stays out of the default view for that reason. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 1211022.
Observations1
Issue DateFebruary 24, 2012
StatusNo Warning Letter
Related Inspections10
Establishment Details
Firm
Pfizer, Inc.
Location
Groton, Connecticut, United States
FEI Number
1211022
Product Type
Drugs
Issue Date
February 24, 2012
Country
United States
Inspection History, 2017 to 2025
NAI7
VAI3
NAI means No Action Indicated. VAI means Voluntary Action Indicated.