FDA Inspection 883233 — Eurotrol B.V.
The FDA completed an inspection of Eurotrol B.V. on May 22, 2014 in Ede Gld. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.
Inspection Details
- Classification
- Official Action Indicated (OAI) (OAI)
- End Date
- May 22, 2014
- Fiscal Year
- 2014
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Ede Gld (Netherlands)