FDA Inspection 635560 — Rommelag CDMO GmbH
The FDA completed an inspection of Rommelag CDMO GmbH on Nov 19, 2009 in Sulzbach-Laufen. 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
- Nov 19, 2009
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Sulzbach-Laufen (Germany)