FDA Inspection 969406 — Pfizer Inc

Pfizer Inc — FEI 1940118

The FDA completed an inspection of Pfizer Inc on February 16, 2016 in Chesterfield, MO. 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
February 16, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Chesterfield, MO (United States)