FDA Inspection 815162 — Skanray Technologies Pvt. Ltd

Skanray Technologies Pvt. Ltd — FEI 3002513440

The FDA completed an inspection of Skanray Technologies Pvt. Ltd on Dec 6, 2012 in Mysore. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 6, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Mysore (India)

Citations

IDCFRDescription
310121 CFR 820.30(g)Design validation- Lack of or inadequate procedures
312521 CFR 820.80(d)Lack of or inadequate final acceptance procedures
313021 CFR 820.100(a)Lack of or inadequate procedures