FDA Inspection 852393 — 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 Sep 26, 2013 in Rietheim-Weilheim. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 26, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Rietheim-Weilheim (Germany)

Citations

IDCFRDescription
311921 CFR 820.75(b)Lack/Inad procedure-Monitoring/Control of Validated Proces

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