FDA Inspection 858436 — Remel Atlanta, A Div. of Remel, Inc.
The FDA completed an inspection of Remel Atlanta, A Div. of Remel, Inc. on November 19, 2013 in Norcross, GA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- November 19, 2013
- Fiscal Year
- 2014
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Norcross, GA (United States)