FDA inspection

Avcor Health Care Products, Inc: FDA inspection ending Jan 12, 2017

FDA inspection 1000480 · No Action Indicated (NAI) · Grand Prairie, TX

Key facts

Inspection ID 1000480
Firm Avcor Health Care Products, Inc
FEI number 3000214907
Address 2750 113th St Ste 300
City Grand Prairie
State TX
ZIP 75050
Country United States
Fiscal year 2017
Inspection end date Jan 12, 2017
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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