# GYMMAX TECHNOLOGY SHENZHEN CO., LTD. – FDA Inspection, Oct 23, 2014

Source: https://www.keypedia.com/records/fda_inspections/gymmax-technology-shenzhen-co-ltd/18533147-857b-4e39-86cc-d2bf3fdc8c81
Source feed: FDA_Inspections

> FDA inspection 902866 of GYMMAX TECHNOLOGY SHENZHEN CO., LTD., October 23, 2014. Classification: Voluntary Action Indicated (VAI). 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 902866
- Company Name: GYMMAX TECHNOLOGY SHENZHEN CO., LTD.
- Inspection Date: 2014-10-23
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- 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 1016646 - 2017-06-15](https://www.keypedia.com/records/fda_inspections/gymmax-technology-shenzhen-co-ltd/f8c43adb-987b-40ef-ad74-2e87650d7b92)

Company: https://www.keypedia.com/companies/gymmax-technology-shenzhen-co-ltd/11b80b64-c502-4065-b291-3c00bd50005c

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