# FDA Inspection 1024996 - Ultratellege USA Co. Ltd. - August 23, 2017

Source: https://www.keypedia.com/records/fda_inspections/ultratellege-usa-co-ltd/d04dd740-be1b-4990-b735-3ef666a8c68e
Source feed: FDA_Inspections

> FDA Inspection 1024996 for Ultratellege USA Co. Ltd. on August 23, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1024996
- Company Name: Ultratellege USA Co. Ltd.
- Inspection Date: 2017-08-23
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/ultratellege-usa-co-ltd/40b446b8-7c25-4121-905c-d9647d30ca5f

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