FDA Inspection 1056362 — Pfizer, Inc.

Pfizer, Inc. — FEI 1211022

The FDA completed an inspection of Pfizer, Inc. on June 21, 2018 in Groton, CT. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 21, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Groton, CT (United States)

Additional Details

Sponsor, Contract Research Organization