# FDA Inspection 797770 - Rigid FX Orthopedics, Inc - August 29, 2012

Source: https://www.keypedia.com/records/fda_inspections/rigid-fx-orthopedics-inc/a51f85cf-6ef4-48e6-bfa7-a694ddf6b2b0
Source feed: FDA_Inspections

> FDA Inspection 797770 for Rigid FX Orthopedics, Inc on August 29, 2012. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 797770
- Company Name: Rigid FX Orthopedics, Inc
- Inspection Date: 2012-08-29
- Classification: Official Action Indicated (OAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 797770 - 2012-08-29](https://www.keypedia.com/records/fda_inspections/rigid-fx-orthopedics-inc/9085f730-b3f3-47ab-a238-60a4b4db64d3)

Company: https://www.keypedia.com/companies/rigid-fx-orthopedics-inc/afe352bf-b83e-4813-8897-e780aa506a7c

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