FDA inspection

SOPRO: FDA inspection ending Jul 21, 2022

FDA inspection 1176361 · Voluntary Action Indicated (VAI) · La Ciotat Cedex

Key facts

Inspection ID 1176361
Firm SOPRO
FEI number 3004084693
Address Iv Zac Athelia
City La Ciotat Cedex
Country France
Fiscal year 2022
Inspection end date Jul 21, 2022
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: 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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