FDA Inspection 1125672 — OPKO Diagnostics, LLC

OPKO Diagnostics, LLC — FEI 3010909452

The FDA completed an inspection of OPKO Diagnostics, LLC on July 1, 2020 in Woburn, MA. 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
July 1, 2020
Fiscal Year
2020
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Woburn, MA (United States)

Additional Details

Sponsor, Contract Research Organization