FDA Inspection 1055329 — Gyrus ACMI, Inc.
The FDA completed an inspection of Gyrus ACMI, Inc. on May 23, 2018 in Redmond, WA. 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
- May 23, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Redmond, WA (United States)