FDA Inspection 1028387 — Recipharm Uppsala AB
The FDA completed an inspection of Recipharm Uppsala AB on June 30, 2017 in Uppsala. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- June 30, 2017
- Fiscal Year
- 2017
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Uppsala (Sweden)