FDA Inspection 1298022 — Kindeva Drug Delivery Limited
The FDA completed an inspection of Kindeva Drug Delivery Limited on Mar 14, 2025 in Loughborough. 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 14, 2025
- Fiscal Year
- 2025
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Loughborough (United Kingdom)
Additional details
Mutual Recognition Agreement (MRA)