FDA Inspection 1094433 — Faxitron Bioptics, LLC

Faxitron Bioptics, LLC — FEI 3004855195

The FDA completed an inspection of Faxitron Bioptics, LLC on April 24, 2019 in Tucson, AZ. 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
April 24, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Tucson, AZ (United States)