Kelyniam Global, Inc.

Form 483

Collinsville, Connecticut, United StatesFEI 3009424796Issued May 30, 2017

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 3009424796.

Observations7

Issue DateMay 30, 2017

StatusNo Warning Letter

Related Inspections6

Establishment Details

Firm: Kelyniam Global, Inc.
Location: Collinsville, Connecticut, United States
FEI Number: 3009424796
Product Type: Devices
Issue Date: May 30, 2017
Country: United States

Inspection History, 2013 to 2024

VAI5

OAI1

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

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Kelyniam Global, Inc. FDA Form 483, Collinsville, Connecticut, May 30, 2017