FDA inspection

Prestige Ameritech: FDA inspection ending Aug 20, 2018

FDA inspection 1063422 · Voluntary Action Indicated (VAI) · North Richland Hills, TX

Key facts

Inspection ID 1063422
Firm Prestige Ameritech
FEI number 3005022483
Address 7201 Iron Horse Blvd
City North Richland Hills
State TX
ZIP 76180
Country United States
Fiscal year 2018
Inspection end date Aug 20, 2018
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes 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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