Gunnell Llc

Form 483

Elk City, Oklahoma, United StatesFEI 3009255757Issued February 18, 2016

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 3009255757.

Observations2

Issue DateFebruary 18, 2016

StatusNo Warning Letter

Related Inspections4

Establishment Details

Firm: Gunnell Llc
Location: Elk City, Oklahoma, United States
FEI Number: 3009255757
Product Type: Devices
Issue Date: February 18, 2016
Country: United States

Inspection History, 2010 to 2016

VAI3

OAI1

VAI means Voluntary Action Indicated. OAI means Official Action Indicated.

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Gunnell Llc FDA Form 483, Elk City, Oklahoma, February 18, 2016