FDA Inspection 884408 — Netech Corp.

Netech Corp. — FEI 1000522032

The FDA completed an inspection of Netech Corp. on April 28, 2014 in Farmingdale, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 28, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Farmingdale, NY (United States)

Citations

IDCFRDescription
316821 CFR 820.198(a)Complaints
383721 CFR 820.25(b)Training records