FDA inspection

G21 Srl: FDA inspection ending May 25, 2017

FDA inspection 1012795 · Voluntary Action Indicated (VAI) · San Possidonio

Key facts

Inspection ID 1012795
Firm G21 Srl
FEI number 3010898856
Address Via Sandro Pertini 8
City San Possidonio
Country Italy
Fiscal year 2017
Inspection end date May 25, 2017
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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