Arch - MedTorque Inc.

Form 483

Kenosha, Wisconsin, United StatesFEI 3005874553Issued March 18, 2010

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 3005874553.

Observations5

Issue DateMarch 18, 2010

StatusNo Warning Letter

Related Inspections4

Establishment Details

Firm: Arch - MedTorque Inc.
Location: Kenosha, Wisconsin, United States
FEI Number: 3005874553
Product Type: Devices
Issue Date: March 18, 2010
Country: United States

Inspection History, 2010 to 2023

NAI2

VAI2

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

Act on This Form 483

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Arch - MedTorque Inc. FDA Form 483, Kenosha, Wisconsin, March 18, 2010