Nomax Inc – FDA Inspection, Sep 17, 2014

Record Details

This FDA Inspection record concerns Nomax Inc, with an inspection on September 17, 2014, issued by the Center for Devices and Radiological Health, covering devices.

Company: Nomax Inc
Inspection Date: September 17, 2014
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 0c2c7622-fa7a-4d9a-a248-16920a8c7c71

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number: 895449
FDA center: Medical Devices & Rad Health
Project area: Compliance: Devices

FDA Citations

21 CFR 820.181DMR - not or inadequately maintained
21 CFR 820.40Lack of procedures, or not maintained
21 CFR 820.80(c)Documentation
21 CFR 820.25(b)Training records
21 CFR 820.80(a)Lack of or inadequate procedures - Acceptance activities
21 CFR 820.100(a)Lack of or inadequate procedures
21 CFR 820.184Lack of or inadequate DHR procedures
21 CFR 820.20(c)Management review - Lack of or inadequate procedures
21 CFR 820.198(a)Lack of or inadequate complaint procedures
21 CFR 820.25(b)Training - Lack of or inadequate procedures

Showing 10 of 18 citations.

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Other FDA inspections of Nomax Inc

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February 25, 2026	Not classified	Kansas City District Office
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June 24, 2022	NAI	Center for Food Safety and Applied Nutrition	Food Composition, Standards, Labeling and Econ
February 1, 2018	VAI	Center for Drug Evaluation and Research	Drug Quality Assurance