FDA Inspection 1234040 — Brochier Technologies

Brochier Technologies — FEI 3030409760

The FDA completed an inspection of Brochier Technologies on Mar 7, 2024 in Villeurbanne. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 7, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Villeurbanne (France)

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