FDA Inspection 1280666 — BAAT MEDICAL PRODUCTS BV

BAAT MEDICAL PRODUCTS BV — FEI 3015216945

The FDA completed an inspection of BAAT MEDICAL PRODUCTS BV on Aug 14, 2025 in Hengelo. 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
Aug 14, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Hengelo (Netherlands)

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