FDA Inspection 1035083 — Amarex Clinical Research, LLC
The FDA completed an inspection of Amarex Clinical Research, LLC on December 5, 2017 in Germantown, MD. 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
- December 5, 2017
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Germantown, MD (United States)
Additional Details
Sponsor, Contract Research Organization