FDA inspection

M.D.L. S.r.l.: FDA inspection ending Sep 19, 2019

FDA inspection 1102625 · Voluntary Action Indicated (VAI) · Delebio

Key facts

Inspection ID 1102625
Firm M.D.L. S.r.l.
FEI number 3004749705
Address Via Tavani N. 1/A
City Delebio
Country Italy
Fiscal year 2019
Inspection end date Sep 19, 2019
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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