FDA Warning Letter — Vidco, Inc.

Case 516295 — FEI 3020646

The FDA took a Warning Letter action against Vidco, Inc. on May 5, 2017 (Beaverton, OR). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Vidco, Inc.
Date
May 5, 2017
Fiscal Year
2017
Product Type
Devices
Center
CDRH
Location
Beaverton, OR (United States)