FDA inspection

Hiossen Inc.: FDA inspection ending Apr 24, 2017

FDA inspection 1038513 · No Action Indicated (NAI) · Norwood, NJ

Key facts

Inspection ID 1038513
Firm Hiossen Inc.
FEI number 3010185635
Address 50 Maple St
City Norwood
State NJ
ZIP 07648
Country United States
Fiscal year 2017
Inspection end date Apr 24, 2017
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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