FDA Inspection 1097508 — Kindeva Drug Delivery Limited
The FDA completed an inspection of Kindeva Drug Delivery Limited on May 3, 2018 in Loughborough. 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
- May 3, 2018
- Fiscal Year
- 2018
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Loughborough (United Kingdom)
Additional Details
Mutual Recognition Agreement (MRA)