FDA inspection

Biomat USA Inc: FDA inspection ending Nov 20, 2017

FDA inspection 1031702 · Voluntary Action Indicated (VAI) · Albuquerque, NM

Key facts

Inspection ID 1031702
Firm Biomat USA Inc
FEI number 1721678
Address 701 2nd St SW
City Albuquerque
State NM
ZIP 87102
Country United States
Fiscal year 2018
Inspection end date Nov 20, 2017
Classification Voluntary Action Indicated (VAI)
Project area Blood and Blood Products
Product type Biologics

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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