FDA inspection

GP Pharm SA: FDA inspection ending Jan 24, 2017

FDA inspection 1004446 · Voluntary Action Indicated (VAI) · Sant Quinti De Mediona

Key facts

Inspection ID 1004446
Firm GP Pharm SA
FEI number 3008345811
Address Poligono Industrial Els Vinyets-Fogars, Sector 2, Carretera Comarcal 244 Km. 22
City Sant Quinti De Mediona
Country Spain
Fiscal year 2017
Inspection end date Jan 24, 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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