Teleflex Medical, Inc.

Form 483

Mansfield, Massachusetts, United StatesFEI 1221601Issued August 27, 2009

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 1221601.

Observations2

Issue DateAugust 27, 2009

StatusNo Warning Letter

Related Inspections3

Establishment Details

Firm: Teleflex Medical, Inc.
Location: Mansfield, Massachusetts, United States
FEI Number: 1221601
Product Type: Devices
Issue Date: August 27, 2009
Country: United States

Inspection History, 2009 to 2017

NAI1

VAI2

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

Act on This Form 483

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Teleflex Medical, Inc. FDA Form 483, Mansfield, Massachusetts, August 27, 2009