FDA Inspection 676052 — Vidco, Inc.

Vidco, Inc. — FEI 3020646

The FDA completed an inspection of Vidco, Inc. on August 18, 2010 in Beaverton, OR. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 18, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Beaverton, OR (United States)

Citations

IDCFRDescription
405921 CFR 820.22Quality Audits - defined intervals