FDA inspection

Almore International Inc: FDA inspection ending Dec 18, 2007

FDA inspection 500309 · No Action Indicated (NAI) · Beaverton, OR

Key facts

Inspection ID 500309
Firm Almore International Inc
FEI number 3018986
Address 10950 SW 5th St Ste 270
City Beaverton
State OR
ZIP 97005-4746
Fiscal year 2008
Inspection end date Dec 18, 2007
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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