FDA Inspection 1100057 — Hubei Biocause Heilen Pharmaceutical Co., Ltd.
The FDA completed an inspection of Hubei Biocause Heilen Pharmaceutical Co., Ltd. on August 16, 2019 in Jingmen. 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
- August 16, 2019
- Fiscal Year
- 2019
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Jingmen (China)