# FDA Inspection 997382 - Vidco, Inc. - January 12, 2017

Source: https://www.keypedia.com/records/fda_inspections/vidco-inc/8949a4cd-4d46-418d-86d0-52dfe25ef663
Source feed: FDA_Inspections

> FDA inspection 997382 of Vidco, Inc., January 12, 2017. Classification: Official Action Indicated (OAI). 10 citations under 21 CFR parts 803, 806 and 820. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 997382
- Company Name: Vidco, Inc.
- Inspection Date: 2017-01-12
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 10

## Related Documents

- FDA Inspection 1040758 - 2018-02-08
- FDA Inspection 864382 - 2014-02-03
- FDA Inspection 789445 - 2012-07-02
- [FDA Inspection 676052 - 2010-08-18](https://www.keypedia.com/records/fda_inspections/vidco-inc/ac425247-63e2-4e72-b1a0-7a958208c5b7)

Company: https://www.keypedia.com/companies/vidco-inc/0b3d709e-71de-4f09-bb8b-7a5ae40e3f55

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7