FDA Inspection 866683 — I.T.S. GmbH

I.T.S. GmbH — FEI 3004369035

The FDA completed an inspection of I.T.S. GmbH on January 30, 2014 in Lasnitzhohe. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 6 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
January 30, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Lasnitzhohe (Austria)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
312321 CFR 820.80(c)Lack of or inadequate In-process acceptance procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
366621 CFR 820.20(c)Management review - Lack of or inadequate procedures
63021 CFR 803.17Lack of Written MDR Procedures