FDA inspection

The Prometheus Group: FDA inspection ending Feb 15, 2017

FDA inspection 1002606 · No Action Indicated (NAI) · Dover, NH

Key facts

Inspection ID 1002606
Firm The Prometheus Group
FEI number 1000513601
Address 1 Washington St Ste 3171
City Dover
State NH
ZIP 03820
Country United States
Fiscal year 2017
Inspection end date Feb 15, 2017
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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