FDA Inspection 1081235 — Guidemia Technologies Inc.
The FDA completed an inspection of Guidemia Technologies Inc. on Feb 11, 2019 in Los Alamitos, CA. 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
- Feb 11, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Los Alamitos, CA (United States)