# Volk Optical Inc – FDA Inspection, Oct 24, 2012

Source: https://www.keypedia.com/records/fda_inspections/volk-optical-inc/b4ca3346-1fb1-4846-a637-9d72b53a3fe3
Source feed: FDA_Inspections

> FDA inspection 809759 of Volk Optical Inc, October 24, 2012. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 809759
- Company Name: Volk Optical Inc
- Inspection Date: 2012-10-24
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- [FDA Inspection 1027501 - 2017-09-28](https://www.keypedia.com/records/fda_inspections/volk-optical-inc/7fcf2e1d-4184-485a-907b-3b487ffdd985)
- FDA Inspection 903132 - 2014-11-06
- FDA Inspection 589876 - 2009-06-26

Company: https://www.keypedia.com/companies/volk-optical-inc/fa891e36-e3d5-409b-a5e2-ad166c62956d

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