FDA Inspection 1197575 — Dimeda Instrumente GmbH

Dimeda Instrumente GmbH — FEI 3002806816

The FDA completed an inspection of Dimeda Instrumente GmbH on Jan 26, 2023 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
Jan 26, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Tuttlingen (Germany)

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