FDA inspection

The Prometheus Group: FDA inspection ending Jun 21, 2012

FDA inspection 787543 · Voluntary Action Indicated (VAI) · Dover, NH

Key facts

Inspection ID 787543
Firm The Prometheus Group
FEI number 1000513601
Address 1 Washington St Ste 3171
City Dover
State NH
ZIP 03820
Country United States
Fiscal year 2012
Inspection end date Jun 21, 2012
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 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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