# Relax Fir Master Inc. – FDA Inspection, Mar 25, 2015

Source: https://www.keypedia.com/records/fda_inspections/relax-fir-master-inc/0f917d5b-234d-49bb-94ad-dcb15e56e38f
Source feed: FDA_Inspections

> FDA inspection 919380 of Relax Fir Master Inc., March 25, 2015. Classification: No Action Indicated (NAI). 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 919380
- Company Name: Relax Fir Master Inc.
- Inspection Date: 2015-03-25
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 717010 - 2011-03-30

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

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