FDA inspection

Biomat USA Inc: FDA inspection ending Dec 18, 2012

FDA inspection 812632 · No Action Indicated (NAI) · Inkster, MI

Key facts

Inspection ID 812632
Firm Biomat USA Inc
FEI number 3005568732
Address 27575 Michigan Ave
City Inkster
State MI
ZIP 48141
Country United States
Fiscal year 2013
Inspection end date Dec 18, 2012
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
  • 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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