FDA Inspection 925969 — Fresenius Kabi AB
The FDA completed an inspection of Fresenius Kabi AB on Mar 20, 2015 in Uppsala. 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: Devices.
Inspection details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Mar 20, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Project Evaluation: Devices
- Location
- Uppsala (Sweden)
Additional details
Postmarket Audit Inspections