FDA inspection

Unitron Hearing Inc: FDA inspection ending Jun 17, 2002

FDA inspection 223476 · No Action Indicated (NAI) · Minneapolis, MN

Key facts

Inspection ID 223476
Firm Unitron Hearing Inc
FEI number 1824293
Address 14755 27th Ave N
City Minneapolis
State MN
ZIP 55447-4866
Fiscal year 2002
Inspection end date Jun 17, 2002
Classification No Action Indicated (NAI)
Project area Compliance: Med Devices
Product type Devices

At a glance

  • None Citations
  • None 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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