FDA Inspection 1243533 — GEBRUDER RENGGLI, AG

GEBRUDER RENGGLI, AG — FEI 3009538961

The FDA completed an inspection of GEBRUDER RENGGLI, AG on Jun 6, 2024 in Schaffhausen. 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
Jun 6, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Schaffhausen (Switzerland)