FDA inspection

Horiba Instruments Incorporated: FDA inspection ending Jan 15, 2010

FDA inspection 627000 · Official Action Indicated (OAI) · Canton, MI

Key facts

Inspection ID 627000
Firm Horiba Instruments Incorporated
FEI number 1827821
Address 5449 Research Dr
City Canton
State MI
ZIP 48188
Country United States
Fiscal year 2010
Inspection end date Jan 15, 2010
Classification Official Action Indicated (OAI)
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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