FDA Inspection 1210857 — Recipharm Uppsala AB
The FDA completed an inspection of Recipharm Uppsala AB on August 26, 2021 in Uppsala. 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 26, 2021
- Fiscal Year
- 2021
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Uppsala (Sweden)
Additional Details
Mutual Recognition Agreement (MRA)