FDA Inspection 1220833 — Zhejiang Peptites Biotech Co.,Ltd.
The FDA completed an inspection of Zhejiang Peptites Biotech Co.,Ltd. on Sep 8, 2023 in Shaoxing. 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
- Sep 8, 2023
- Fiscal Year
- 2023
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Shaoxing (China)