FDA Inspection 789445 — Vidco, Inc.

Vidco, Inc. — FEI 3020646

The FDA completed an inspection of Vidco, Inc. on July 2, 2012 in Beaverton, OR. 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
July 2, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Beaverton, OR (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
313021 CFR 820.100(a)Lack of or inadequate procedures