FDA inspection

BIT Group France: FDA inspection ending Feb 16, 2012

FDA inspection 776352 · No Action Indicated (NAI) · Montpellier Cedex 5

Key facts

Inspection ID 776352
Firm BIT Group France
FEI number 3006946274
Address C2 Diagnostic, Parc Euromedecine Ii; Rue De La Valsiere; Cs 14287 Grabels
City Montpellier Cedex 5
Country France
Fiscal year 2012
Inspection end date Feb 16, 2012
Classification No Action Indicated (NAI)
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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