FDA inspection

Angstrom Manufacturing, Inc.: FDA inspection ending Jun 8, 2011

FDA inspection 729505 · Voluntary Action Indicated (VAI) · Sainte Genevieve, MO

Key facts

Inspection ID 729505
Firm Angstrom Manufacturing, Inc.
FEI number 3003610374
Address 4 Trautman Industrial Ct
City Sainte Genevieve
State MO
ZIP 63670
Country United States
Fiscal year 2011
Inspection end date Jun 8, 2011
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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