FDA Inspection 1330614 — Pfizer Asia Manufacturing Pte Ltd.

Pfizer Asia Manufacturing Pte Ltd. — FEI 3003901862

The FDA completed an inspection of Pfizer Asia Manufacturing Pte Ltd. on Oct 18, 2023 in Singapore. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 18, 2023
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Singapore (Singapore)

Additional Details

Mutual Recognition Agreement (MRA)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.