# FDA Inspection 939551 - Ortho Technology, Inc. - August 26, 2015

Source: https://www.keypedia.com/records/fda_inspections/ortho-technology-inc/6aa573fc-7178-43fb-99b2-784c9a97635e
Source feed: FDA_Inspections

> FDA Inspection 939551 for Ortho Technology, Inc. on August 26, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 939551
- Company Name: Ortho Technology, Inc.
- Inspection Date: 2015-08-26
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 939551 - 2015-08-26](https://www.keypedia.com/records/fda_inspections/ortho-technology-inc/5afb0aad-0a5b-46d4-a652-b565a96fd083)
- [FDA Inspection 810549 - 2012-12-13](https://www.keypedia.com/records/fda_inspections/ortho-technology-inc/cfb6b9c3-ae73-4f0b-8528-2594969fb093)
- [FDA Inspection 810549 - 2012-12-13](https://www.keypedia.com/records/fda_inspections/ortho-technology-inc/638eeb94-f2ea-49ae-8ef7-4c08389a47fb)

Company: https://www.keypedia.com/companies/ortho-technology-inc/3754201f-102c-4a9c-8a3d-0286358f943c

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