FDA Inspection 1238552 — Sterigenics Germany GmbH

Sterigenics Germany GmbH — FEI 3006003617

The FDA completed an inspection of Sterigenics Germany GmbH on May 15, 2024 in Wiesbaden. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
May 15, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Wiesbaden (Germany)