# FDA Inspection 950683 - Orthorebirth Co Ltd - November 19, 2015

Source: https://www.keypedia.com/records/fda_inspections/orthorebirth-co-ltd/637ea4c1-fb6e-4b16-9779-8cd0ad4cf348
Source feed: FDA_Inspections

> FDA Inspection 950683 for Orthorebirth Co Ltd on November 19, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 950683
- Company Name: Orthorebirth Co Ltd
- Inspection Date: 2015-11-19
- 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/orthorebirth-co-ltd/c988daf8-a7c9-412b-b25d-ac3de7d47134

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