FDA Inspection 654321 — Acist Medical Systems
The FDA completed an inspection of Acist Medical Systems on Mar 24, 2010 in Eden Prairie, MN. 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
- Mar 24, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Eden Prairie, MN (United States)