FDA Inspection 977394 — Gyrus ACMI, Inc.
The FDA completed an inspection of Gyrus ACMI, Inc. on Jul 1, 2016 in Bartlett, TN. 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
- Jul 1, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Bartlett, TN (United States)