Nomax, INC

Form 483FOIA Uncovered

Saint Louis, MissouriFEI 1937310Issued February 01, 2018

View FDA's Record for This Firm

Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 1937310.

ObservationsNot available

Issue DateFebruary 01, 2018

StatusNo Warning Letter

Related Inspections10

Establishment Details

Firm: Nomax, INC
Location: Saint Louis, Missouri
FEI Number: 1937310
Product Type: Devices
Issue Date: February 01, 2018
Country: United States

Inspection History, 2010 to 2026

NAI5

VAI4

OAI1

NAI means No Action Indicated. VAI means Voluntary Action Indicated. OAI means Official Action Indicated.

Act on This Form 483

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Nomax, INC FDA Form 483, Saint Louis, Missouri, February 1, 2018