FDA Inspection 1120343 — Theragen, Inc

Theragen, Inc — FEI 3013378804

The FDA completed an inspection of Theragen, Inc on February 20, 2020 in Jacksonville, FL. 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
February 20, 2020
Fiscal Year
2020
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Jacksonville, FL (United States)