FDA Inspection 1266715 — Steripac GmbH

Steripac GmbH — FEI 3009217531

The FDA completed an inspection of Steripac GmbH on March 19, 2025 in Calw. 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
March 19, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Calw (Germany)