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FDA Inspection
•Vidco, Inc.•August 18, 2010

FDA Inspection 676052 - Vidco, Inc. - August 18, 2010

Record Details

This FDA Inspection record concerns Vidco, Inc., with an inspection on August 18, 2010, issued by the Center for Devices and Radiological Health, covering devices.

Company
Vidco, Inc.
Inspection Date
August 18, 2010
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · ac425247-63e2-4e72-b1a0-7a958208c5b7

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
676052
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

FDA Citations

1
  1. 21 CFR 820.22Quality Audits - defined intervals

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Vidco, Inc.

4
DateClassificationOfficeProject area
February 8, 2018NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
January 12, 2017OAICenter for Devices and Radiological HealthCompliance: Devices
February 3, 2014NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
July 2, 2012VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Vidco, Inc.
  • FDA Inspection 1040758 - 2018-02-08
  • FDA Inspection 997382 - 2017-01-12
  • FDA Inspection 864382 - 2014-02-03
  • FDA Inspection 789445 - 2012-07-02

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