# Galix Biomedical Instrumentation, Inc. – FDA Inspection, Jul 3, 2017

Source: https://www.keypedia.com/records/fda_inspections/galix-biomedical-instrumentation-inc/d43d788f-a307-4ce0-aa1c-eb4daa3d37ce
Source feed: FDA_Inspections

> FDA inspection 1016788 of Galix Biomedical Instrumentation, Inc., July 03, 2017. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR parts 803 and 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1016788
- Company Name: Galix Biomedical Instrumentation, Inc.
- Inspection Date: 2017-07-03
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 6

## Related Documents

- [FDA Inspection 832712 - 2013-05-21](https://www.keypedia.com/records/fda_inspections/galix-biomedical-instrumentation-inc/76fe32ad-9cd4-4298-aa30-c04d3a5fedf4)
- FDA Inspection 615917 - 2009-09-21

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/karen-m-cruz-arenas/6c698301-84ca-4ba7-a79c-309721db2f1b)

Company: https://www.keypedia.com/companies/galix-biomedical-instrumentation-inc/2ead02e9-31cf-4027-b904-dd137af1b7e0

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