FDA inspection

Konica Minolta Healthcare, Americas, Inc.: FDA inspection ending Aug 25, 2017

FDA inspection 1022872 · Voluntary Action Indicated (VAI) · Garner, NC

Key facts

Inspection ID 1022872
Firm Konica Minolta Healthcare, Americas, Inc.
FEI number 3002885429
Address 2217 Us Highway 70 E
City Garner
State NC
ZIP 27529
Country United States
Fiscal year 2017
Inspection end date Aug 25, 2017
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: 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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