FDA Inspection 1217595 — Biomat USA, Inc

Biomat USA, Inc — FEI 3005488132

The FDA completed an inspection of Biomat USA, Inc on Sep 13, 2023 in City Of Industry, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 13, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
City Of Industry, CA (United States)

Citations

IDCFRDescription
63021 CFR 803.17Lack of Written MDR Procedures

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.