# FDA Inspection 920198 - Genemax Medical Products Industry Corp. - March 17, 2015

Source: https://www.keypedia.com/records/fda_inspections/genemax-medical-products-industry-corp/3fb5f2c1-4c1c-4a19-85fc-22a915eed0fe
Source feed: FDA_Inspections

> FDA Inspection 920198 for Genemax Medical Products Industry Corp. on March 17, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 920198
- Company Name: Genemax Medical Products Industry Corp.
- Inspection Date: 2015-03-17
- 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 920198 - 2015-03-17](https://www.keypedia.com/records/fda_inspections/genemax-medical-products-industry-corp/c9f1756a-6c4f-4663-a4c4-a0ba7d8db744)

Company: https://www.keypedia.com/companies/genemax-medical-products-industry-corp/4f6d0a40-b064-4ade-a4f6-358e4408306c

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