# FDA Inspection 976677 - Vioptix, Inc. - April 13, 2016

Source: https://www.keypedia.com/records/fda_inspections/vioptix-inc/e5e51fe5-6123-4841-8dfe-46439cafaf5a
Source feed: FDA_Inspections

> FDA Inspection 976677 for Vioptix, Inc. on April 13, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 976677
- Company Name: Vioptix, Inc.
- Inspection Date: 2016-04-13
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 843139 - 2013-08-05](https://www.keypedia.com/records/fda_inspections/vioptix-inc/c2e452f9-1222-40e6-ab20-8fcdd5e13015)
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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