FDA inspection

Cefla s.c.: FDA inspection ending Jul 20, 2018

FDA inspection 1061484 · Voluntary Action Indicated (VAI) · Imola

Key facts

Inspection ID 1061484
Firm Cefla s.c.
FEI number 3006610845
Address Via Bicocca 14/C
City Imola
Country Italy
Fiscal year 2018
Inspection end date Jul 20, 2018
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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