FDA Inspection 891089 — MAXTER CATHETERS
The FDA completed an inspection of MAXTER CATHETERS on July 31, 2014 in Marseille. 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
- July 31, 2014
- Fiscal Year
- 2014
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Marseille (France)