# FDA Inspection 670001 - Ultralight Optics, Inc - July 01, 2010

Source: https://www.keypedia.com/records/fda_inspections/ultralight-optics-inc/6b030deb-1e26-411a-88bc-5885c20605af
Source feed: FDA_Inspections

> FDA Inspection 670001 for Ultralight Optics, Inc on July 01, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 670001
- Company Name: Ultralight Optics, Inc
- Inspection Date: 2010-07-01
- 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/ultralight-optics-inc/fb0d746d-3bf8-447c-912f-e9dc121f18c2

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