# FDA Inspection 971960 - Ultralite Enterprises Inc - May 12, 2016

Source: https://www.keypedia.com/records/fda_inspections/ultralite-enterprises-inc/6ae32cbb-a7a9-4270-913c-e3e13d111ff8
Source feed: FDA_Inspections

> FDA Inspection 971960 for Ultralite Enterprises Inc on May 12, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 971960
- Company Name: Ultralite Enterprises Inc
- Inspection Date: 2016-05-12
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/ultralite-enterprises-inc/38d8b2bf-c1f4-4e43-bfdd-6f1ea477254b

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