FDA inspection

Vygon MFG, Inc.: FDA inspection ending Feb 22, 2006

FDA inspection 416816 · No Action Indicated (NAI) · Dover, NH

Key facts

Inspection ID 416816
Firm Vygon MFG, Inc.
FEI number 1000120555
Address 87 Venture Dr
City Dover
State NH
ZIP 03820-5914
Fiscal year 2006
Inspection end date Feb 22, 2006
Classification No Action Indicated (NAI)
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Product type Devices, Drugs

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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