FDA Inspection 1232698 — Dufner Instrumente GmbH

Dufner Instrumente GmbH — FEI 3002806862

The FDA completed an inspection of Dufner Instrumente GmbH on Mar 13, 2024 in Tuttlingen. 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 13, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Tuttlingen (Germany)

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