FDA Inspection
Volk Optical IncVolk Optical Inc – FDA Inspection, Oct 24, 2012
Record Details
This FDA Inspection record concerns Volk Optical Inc, with an inspection on October 24, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Volk Optical Inc
- Inspection Date
- October 24, 2012
- Product Type
- Devices
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ID · b4ca3346-1fb1-4846-a637-9d72b53a3fe3
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 809759
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures
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Other FDA inspections of Volk Optical Inc
3| Date | Classification | Office | Project area |
|---|---|---|---|
| September 28, 2017 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| November 6, 2014 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| June 26, 2009 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Volk Optical Inc
- FDA Inspection 1027501 - 2017-09-28
- FDA Inspection 903132 - 2014-11-06
- FDA Inspection 589876 - 2009-06-26
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