# FDA Inspection 822950 - Ortho-Cycle Company Inc. - March 13, 2013

Source: https://www.keypedia.com/records/fda_inspections/ortho-cycle-company-inc/bdd6fb0a-2770-41d7-a52d-9603f67a9e9e
Source feed: FDA_Inspections

> FDA Inspection 822950 for Ortho-Cycle Company Inc. on March 13, 2013. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 822950
- Company Name: Ortho-Cycle Company Inc.
- Inspection Date: 2013-03-13
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 878180 - 2014-05-06](https://www.keypedia.com/records/fda_inspections/ortho-cycle-company-inc/7376e2be-a114-462b-9d8f-d1041ad09f5f)
- [FDA Inspection 822950 - 2013-03-13](https://www.keypedia.com/records/fda_inspections/ortho-cycle-company-inc/c1580075-de8c-43f7-bfe1-d626d378d6b7)

Company: https://www.keypedia.com/companies/ortho-cycle-company-inc/6774eac8-af91-4fab-97fb-69e086e9bd4e

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