FDA inspection

Paragon BioTeck Inc: FDA inspection ending Sep 25, 2019

FDA inspection 1109013 · No Action Indicated (NAI) · Portland, OR

Key facts

Inspection ID 1109013
Firm Paragon BioTeck Inc
FEI number 3009934432
Address 4640 Sw Macadam Ave Ste 80
City Portland
State OR
ZIP 97239
Country United States
Fiscal year 2019
Inspection end date Sep 25, 2019
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • Yes 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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