FDA inspection

MilliporeSigma: FDA inspection ending Sep 2, 2009

FDA inspection 610581 · Voluntary Action Indicated (VAI) · Saint Louis, MO

Key facts

Inspection ID 610581
Firm MilliporeSigma
FEI number 1000138378
Address 3050 Spruce St
City Saint Louis
State MO
ZIP 63103
Country United States
Fiscal year 2009
Inspection end date Sep 2, 2009
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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