FDA Inspection 1272814 — Baitella AG

Baitella AG — FEI 3001415205

The FDA completed an inspection of Baitella AG on May 15, 2025 in Zurich. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 15, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Zurich (Switzerland)