# Bloomex International, Inc. – FDA Inspection, May 1, 2009

Source: https://www.keypedia.com/records/fda_inspections/bloomex-international-inc/fa7e51ca-ce12-4a5f-909e-b6168528fd32
Source feed: FDA_Inspections

> FDA inspection 584472 of Bloomex International, Inc., May 01, 2009. Classification: Voluntary Action Indicated (VAI). 9 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: 584472
- Company Name: Bloomex International, Inc.
- Inspection Date: 2009-05-01
- 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: 9

## Related Documents

- [FDA Inspection 790206 - 2012-07-02](https://www.keypedia.com/records/fda_inspections/bloomex-international-inc/f2ef433b-a5ba-47de-b889-eb6c3955260b)

Company: https://www.keypedia.com/companies/bloomex-international-inc/10a4b55e-229a-4f0f-90a9-65bfe3ec5aaf

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