FDA inspection

Biomat USA, Inc.: FDA inspection ending Sep 20, 2017

FDA inspection 1028343 · No Action Indicated (NAI) · Wichita Falls, TX

Key facts

Inspection ID 1028343
Firm Biomat USA, Inc.
FEI number 3002793370
Address 1908 9th St Ste D
City Wichita Falls
State TX
ZIP 76301
Country United States
Fiscal year 2017
Inspection end date Sep 20, 2017
Classification No Action Indicated (NAI)
Project area Blood and Blood Products
Product type Biologics

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 10–99 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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