FDA Inspection 1158863 — Amarex Clinical Research, LLC

Amarex Clinical Research, LLC — FEI 3007940998

The FDA completed an inspection of Amarex Clinical Research, LLC on November 3, 2021 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
November 3, 2021
Fiscal Year
2022
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Germantown, MD (United States)

Additional Details

Sponsor, Contract Research Organization