FDA Inspection 1095074 — Yichang Humanwell Oral Solid Dosage Plant
The FDA completed an inspection of Yichang Humanwell Oral Solid Dosage Plant on June 28, 2019 in Yichang. 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 28, 2019
- Fiscal Year
- 2019
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Yichang (China)