Protech Professional Products, Inc.

Form 483

Boynton Beach, Florida, United StatesFEI 1000137415Issued October 28, 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 1000137415.

Observations7

Issue DateOctober 28, 2016

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: October 28, 2016
Country: United States

Inspection History, 2013 to 2016

VAI2

OAI1

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

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Protech Professional Products, Inc. FDA Form 483, Boynton Beach, Florida, October 28, 2016