FDA Inspection 1265731 — Hilda A. Mujuru
The FDA completed an inspection of Hilda A. Mujuru on March 21, 2025 in Harare. 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
- March 21, 2025
- Fiscal Year
- 2025
- Product Type
- Drugs
- Project Area
- Bioresearch Monitoring
- Location
- Harare (Zimbabwe)
Additional Details
Clinical BA/BE