FDA inspection

ANT North America Inc: FDA inspection ending Dec 7, 2012

FDA inspection 811279 · Voluntary Action Indicated (VAI) · Philadelphia, PA

Key facts

Inspection ID 811279
Firm ANT North America Inc
FEI number 3007707546
Address 1617 John F Kennedy Blvd Ste 821
City Philadelphia
State PA
ZIP 19103
Country United States
Fiscal year 2013
Inspection end date Dec 7, 2012
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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