FDA inspection

Intermetro Industries Corp.: FDA inspection ending Sep 29, 2014

FDA inspection 897767 · No Action Indicated (NAI) · Wilkes Barre, PA

Key facts

Inspection ID 897767
Firm Intermetro Industries Corp.
FEI number 3001600991
Address 651 N Washington St
City Wilkes Barre
State PA
ZIP 18705
Country United States
Fiscal year 2014
Inspection end date Sep 29, 2014
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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