# Volk Optical Inc – FDA Inspection, Sep 28, 2017

Source: https://www.keypedia.com/records/fda_inspections/volk-optical-inc/7fcf2e1d-4184-485a-907b-3b487ffdd985
Source feed: FDA_Inspections

> FDA inspection 1027501 of Volk Optical Inc, September 28, 2017. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1027501
- Company Name: Volk Optical Inc
- Inspection Date: 2017-09-28
- 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: 5

## Related Documents

- FDA Inspection 903132 - 2014-11-06
- [FDA Inspection 809759 - 2012-10-24](https://www.keypedia.com/records/fda_inspections/volk-optical-inc/b4ca3346-1fb1-4846-a637-9d72b53a3fe3)
- FDA Inspection 589876 - 2009-06-26

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/benjamin-j-dastoli/688c2ad7-f7ac-47eb-8ca2-4efcd221f636)

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