FDA inspection

PRO-TECH Design & Mfg., Inc.: FDA inspection ending Dec 11, 2014

FDA inspection 906565 · No Action Indicated (NAI) · Arlington, TX

Key facts

Inspection ID 906565
Firm PRO-TECH Design & Mfg., Inc.
FEI number 3010531069
Address 4041 Express St
City Arlington
State TX
ZIP 76001
Country United States
Fiscal year 2015
Inspection end date Dec 11, 2014
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

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

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

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

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