# FDA Inspection 781822 - Gyrx, LLC - April 27, 2012

Source: https://www.keypedia.com/records/fda_inspections/gyrx-llc/229c69c5-2d85-4349-b0d4-e6e4fa44b956
Source feed: FDA_Inspections

> FDA Inspection 781822 for Gyrx, LLC on April 27, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 781822
- Company Name: Gyrx, LLC
- Inspection Date: 2012-04-27
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 781822 - 2012-04-27](https://www.keypedia.com/records/fda_inspections/gyrx-llc/edf0cd21-b0ce-42bf-90aa-bd4d9fc1e66d)

Company: https://www.keypedia.com/companies/gyrx-llc/ef4565bf-602e-47fd-8b9a-0aec7c8ae428

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