FDA inspection

NerPharMa S.r.l.: FDA inspection ending Mar 5, 2015

FDA inspection 920306 · Voluntary Action Indicated (VAI) · Nerviano

Key facts

Inspection ID 920306
Firm NerPharMa S.r.l.
FEI number 3004762406
Address Bldgs 65 And 71 Casella Postale N. 11, Viale Luigi Pasteur 10
City Nerviano
Country Italy
Fiscal year 2015
Inspection end date Mar 5, 2015
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

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
  • 10–99 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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