FDA inspection

Plastiape Spa: FDA inspection ending Jul 30, 2015

FDA inspection 939719 · Voluntary Action Indicated (VAI) · Osnago

Key facts

Inspection ID 939719
Firm Plastiape Spa
FEI number 3003805036
Address Via Primo Maggio 8
City Osnago
Country Italy
Fiscal year 2015
Inspection end date Jul 30, 2015
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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