FDA Inspection 1258115 — KLS Martin SE & Co. KG

KLS Martin SE & Co. KG — FEI 3002807464

The FDA completed an inspection of KLS Martin SE & Co. KG on Apr 9, 2025 in Muhlheim An Der Donau. 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
Apr 9, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Muhlheim An Der Donau (Germany)

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