FDA Inspection 1001171 — ELEGLANCE CORP
The FDA completed an inspection of ELEGLANCE CORP on Dec 7, 2016 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
- Dec 7, 2016
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Duluth, GA (United States)