FDA inspection

LPG Systems: FDA inspection ending May 18, 2017

FDA inspection 1031751 · Voluntary Action Indicated (VAI) · Valence Cedex 9

Key facts

Inspection ID 1031751
Firm LPG Systems
FEI number 3003454229
Address Lpg Systems, 30 Rue Docteur Henri Abel; Cs 90035
City Valence Cedex 9
Country France
Fiscal year 2017
Inspection end date May 18, 2017
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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