FDA Inspection 826405 — Fei Fah Medical Manufacturing Pte. Ltd.
The FDA completed an inspection of Fei Fah Medical Manufacturing Pte. Ltd. on Mar 8, 2013 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
- Mar 8, 2013
- Fiscal Year
- 2013
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Singapore (Singapore)