FDA Inspection 1266715 — Steripac GmbH

Steripac GmbH — FEI 3009217531

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

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