FDA Inspection 967580 — S.U. A. Martin GmbH & Co. KG

S.U. A. Martin GmbH & Co. KG — FEI 3000178338

The FDA completed an inspection of S.U. A. Martin GmbH & Co. KG on Mar 2, 2016 in Rietheim-Weilheim. 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 2, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Rietheim-Weilheim (Germany)

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