# M&M QUALTECH – FDA Inspection, Apr 16, 2010

Source: https://www.keypedia.com/records/fda_inspections/mm-qualtech/0602a8b1-e73c-4d34-883e-b11bb74dbafa
Source feed: FDA_Inspections

> FDA inspection 661810 of M&M QUALTECH, April 16, 2010. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 661810
- Company Name: M&M QUALTECH
- Inspection Date: 2010-04-16
- 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: 4

## Related Documents

- FDA Inspection 1075821 - 2018-11-28

Company: https://www.keypedia.com/companies/mm-qualtech/f194ebd7-82e8-47f7-8a0b-f8ecb2dc8e09

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