# FDA Inspection 717010 - Relax Fir Master Inc. - March 30, 2011

Source: https://www.globalkeysolutions.net/records/fda_inspections/relax-fir-master-inc/df15693b-602e-444e-9984-289abcc00bea
Source feed: FDA_Inspections

> FDA Inspection 717010 for Relax Fir Master Inc. on March 30, 2011. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 717010
- Company Name: Relax Fir Master Inc.
- Inspection Date: 2011-03-30
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 919380 - 2015-03-25](https://www.globalkeysolutions.net/records/fda_inspections/relax-fir-master-inc/0f917d5b-234d-49bb-94ad-dcb15e56e38f)
- [FDA Inspection 717010 - 2011-03-30](https://www.globalkeysolutions.net/records/fda_inspections/relax-fir-master-inc/66339d83-c02d-4c2f-982a-89dbceeff839)

Company: https://www.globalkeysolutions.net/companies/relax-fir-master-inc/c99d5adb-9839-45f1-83d1-7937cff7736a

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