FDA inspection

Biomerieux Inc: FDA inspection ending Jan 25, 2017

FDA inspection 1000732 · Voluntary Action Indicated (VAI) · Hazelwood, MO

Key facts

Inspection ID 1000732
Firm Biomerieux Inc
FEI number 1950204
Address 595 Anglum Rd
City Hazelwood
State MO
ZIP 63042
Country United States
Fiscal year 2017
Inspection end date Jan 25, 2017
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
  • 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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