FDA Inspection 637041 — Abbott Vascular Instruments Deutschland Gmbh
The FDA completed an inspection of Abbott Vascular Instruments Deutschland Gmbh on November 12, 2009 in Rangendingen. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- November 12, 2009
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Rangendingen (Germany)
Additional Details
Postmarket Audit Inspections