# Vioptix, Inc. – FDA Inspection, Jul 21, 2010

Source: https://www.keypedia.com/records/fda_inspections/vioptix-inc/432c16e7-5753-49c9-b8eb-1ffdeaaed85d
Source feed: FDA_Inspections

> FDA inspection 671857 of Vioptix, Inc., July 21, 2010. Classification: No Action Indicated (NAI). 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 671857
- Company Name: Vioptix, Inc.
- Inspection Date: 2010-07-21
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1218185 - 2023-08-21
- FDA Inspection 976677 - 2016-04-13
- FDA Inspection 843139 - 2013-08-05

Company: https://www.keypedia.com/companies/vioptix-inc/f672a512-98c2-4c66-b69b-c8787a176a64

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