# FDA Inspection 710588 - Gleemex Inc. - February 07, 2011

Source: https://www.keypedia.com/records/fda_inspections/gleemex-inc/1f5b5d7e-0e51-455b-a3c0-273e687da289
Source feed: FDA_Inspections

> FDA Inspection 710588 for Gleemex Inc. on February 07, 2011. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 710588
- Company Name: Gleemex Inc.
- Inspection Date: 2011-02-07
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 710588 - 2011-02-07](https://www.keypedia.com/records/fda_inspections/gleemex-inc/d7b52b14-1526-4d9c-8b8d-a81efd4b55cb)
- [FDA Inspection 561243 - 2009-01-28](https://www.keypedia.com/records/fda_inspections/gleemex-inc/39ee9409-6cdd-4c08-bb83-a7993e4577a1)

Company: https://www.keypedia.com/companies/gleemex-inc/17da3fc1-3be7-4f38-ada4-cfde98c68799

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