FDA Inspection 1251480 — Rechon Life Science AB
The FDA completed an inspection of Rechon Life Science AB on September 6, 2024 in Limhamn. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Drugs.
Inspection Details
- Classification
- Official Action Indicated (OAI) (OAI)
- End Date
- September 6, 2024
- Fiscal Year
- 2024
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Limhamn (Sweden)