FDA Inspection 568201 — Gambro Lundia AB
The FDA completed an inspection of Gambro Lundia AB on Mar 5, 2009 in Lund. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection details
- Classification
- No Action Indicated (NAI)
- End Date
- Mar 5, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Lund (Sweden)