# FDA Inspection 895188 - Qualigen Inc - September 16, 2014

Source: https://www.keypedia.com/records/fda_inspections/qualigen-inc/49eeeeef-8e35-4245-ac56-5e7c93dd52db
Source feed: FDA_Inspections

> FDA Inspection 895188 for Qualigen Inc on September 16, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 895188
- Company Name: Qualigen Inc
- Inspection Date: 2014-09-16
- 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 895188 - 2014-09-16](https://www.keypedia.com/records/fda_inspections/qualigen-inc/9d6d65bc-d382-4759-a94a-988dc1d96ce1)
- [FDA Inspection 727211 - 2011-06-02](https://www.keypedia.com/records/fda_inspections/qualigen-inc/e4b24b1b-d754-4825-ac5d-aa48433aa2bb)
- [FDA Inspection 727211 - 2011-06-02](https://www.keypedia.com/records/fda_inspections/qualigen-inc/54d1e48e-8582-4165-8141-9d4aba15f3ed)

Company: https://www.keypedia.com/companies/qualigen-inc/8a352162-a7bc-4e76-844b-47ea4b1e2715

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