FDA Inspection 1211473 — Biorez, Inc

Biorez, Inc — FEI 3019101334

The FDA completed an inspection of Biorez, Inc on August 4, 2023 in New Haven, CT. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 4, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
New Haven, CT (United States)

Citations

IDCFRDescription
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures