FDA inspection

Klockner Of North America: FDA inspection ending Oct 3, 2012

FDA inspection 802887 · Voluntary Action Indicated (VAI) · Miami, FL

Key facts

Inspection ID 802887
Firm Klockner Of North America
FEI number 3011395139
Address 160 Commonwealth Ave Ste L10
City Miami
State FL
ZIP 33130
Country United States
Fiscal year 2013
Inspection end date Oct 3, 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

Browse all FDA inspections