FDA inspection

Herniamesh S.r.l: FDA inspection ending Nov 5, 2009

FDA inspection 626883 · Voluntary Action Indicated (VAI) · Chivasso

Key facts

Inspection ID 626883
Firm Herniamesh S.r.l
FEI number 3005404334
Address Via Fratelli Meliga 1/C
City Chivasso
Country Italy
Fiscal year 2010
Inspection end date Nov 5, 2009
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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