FDA Inspection 584784 — Gyrus ACMI, Inc.
The FDA completed an inspection of Gyrus ACMI, Inc. on May 29, 2009 in Brooklyn Park, MN. 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
- May 29, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Brooklyn Park, MN (United States)
Additional Details
Postmarket Audit Inspections