FDA Inspection
M&M QUALTECHM&M QUALTECH – FDA Inspection, Apr 16, 2010
Record Details
This FDA Inspection record concerns M&M QUALTECH, with an inspection on April 16, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- M&M QUALTECH
- Inspection Date
- April 16, 2010
- Product Type
- Devices
View Company Profile
ID · 0602a8b1-e73c-4d34-883e-b11bb74dbafa
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 661810
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
4- 21 CFR 820.70(f)Buildings
- 21 CFR 820.90(a)Specific non-conforming product procedures
- 21 CFR 820.184DHR content
- 21 CFR 820.184(e)ID label, labeling
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Other FDA inspections of M&M QUALTECH
1| Date | Classification | Office | Project area |
|---|---|---|---|
| November 28, 2018 | Not classified | Office of Inspections and Investigations |
Other documents for M&M QUALTECH
- FDA Inspection 1075821 - 2018-11-28
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