FDA inspection

ABS Corporation: FDA inspection ending May 19, 2014

FDA inspection 879566 · Voluntary Action Indicated (VAI) · Omaha, NE

Key facts

Inspection ID 879566
Firm ABS Corporation
FEI number 1950042
Address 7031 N 16th St
City Omaha
State NE
ZIP 68112
Country United States
Fiscal year 2014
Inspection end date May 19, 2014
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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