Gyrus ACMI, Inc.

Form 483

Bartlett, Tennessee, United StatesFEI 1037007Issued September 18, 2013

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 1037007.

Observations4

Issue DateSeptember 18, 2013

StatusNo Warning Letter

Related Inspections4

Establishment Details

Firm: Gyrus ACMI, Inc.
Location: Bartlett, Tennessee, United States
FEI Number: 1037007
Product Type: Devices
Issue Date: September 18, 2013
Country: United States

Inspection History, 2010 to 2022

NAI3

VAI1

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

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Gyrus ACMI, Inc. FDA Form 483, Bartlett, Tennessee, September 18, 2013