FEI establishment

Protech Professional Products, Inc.

FDA establishment FEI 1000137415 · Boynton Beach, United States

Key facts

FEI number 1000137415
Legal name Protech Professional Products, Inc.
City Boynton Beach
Country United States
Product types Devices
Last inspection Oct 28, 2016

At a glance

  • 1–9 FDA inspections
  • None No Action Indicated (NAI)
  • 1–9 Voluntary Action Indicated (VAI)
  • 1–9 Official Action Indicated (OAI)
  • 1–9 Inspections with a Form 483
  • 10–99 Citations
  • 10–99 Repeat citations
  • 1–9 Warning letters
  • 1–9 Linked 510(k)s

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA establishments (FEI)

An FEI (FDA Establishment Identifier) is the number the FDA assigns to a site it inspects. FEIs of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection and compliance data

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