FDA Inspection 931561 — INTERVASCULAR, SAS
The FDA completed an inspection of INTERVASCULAR, SAS on Jun 18, 2015 in La Ciotat Cedex. 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
- Jun 18, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- La Ciotat Cedex (France)