FDA Inspection 1323728 — OD-OS GmbH

OD-OS GmbH — FEI 3008252121

The FDA completed an inspection of OD-OS GmbH on May 21, 2026 in Teltow. 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
May 21, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Teltow (Germany)

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