FDA Inspection 1056889 — Carelife Usa Inc
The FDA completed an inspection of Carelife Usa Inc on Apr 17, 2018 in Duluth, GA. 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
- Apr 17, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Duluth, GA (United States)