# FDA Inspection 1017591 - KREWE DU OPTIC - November 01, 2016

Source: https://www.keypedia.com/records/fda_inspections/krewe-du-optic/e4e2ac88-b814-4f65-9c54-97833111335e
Source feed: FDA_Inspections

> FDA Inspection 1017591 for KREWE DU OPTIC on November 01, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1017591
- Company Name: KREWE DU OPTIC
- Inspection Date: 2016-11-01
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/krewe-du-optic/31f32651-7e63-4231-9921-8d80b44f9aee

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