Protech Professional Products, Inc.

Form 483

Boynton Beach, Florida, United StatesFEI 1000137415Issued February 27, 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 1000137415.

Observations11

Issue DateFebruary 27, 2013

StatusNo Warning Letter

Related Inspections3

Establishment Details

Firm: Protech Professional Products, Inc.
Location: Boynton Beach, Florida, United States
FEI Number: 1000137415
Product Type: Devices
Issue Date: February 27, 2013
Country: United States

Inspection History, 2013 to 2016

VAI2

OAI1

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

Act on This Form 483

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Protech Professional Products, Inc. FDA Form 483, Boynton Beach, Florida, February 27, 2013