# Gleemex Inc. – FDA Inspection, Jan 28, 2009

Source: https://www.keypedia.com/records/fda_inspections/gleemex-inc/39ee9409-6cdd-4c08-bb83-a7993e4577a1
Source feed: FDA_Inspections

> FDA inspection 561243 of Gleemex Inc., January 28, 2009. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 803 and 820. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 561243
- Company Name: Gleemex Inc.
- Inspection Date: 2009-01-28
- 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: 2

## Related Documents

- FDA Inspection 710588 - 2011-02-07

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