FDA inspection

NerPharMa S.r.l.: FDA inspection ending Oct 26, 2018

FDA inspection 1072258 · No Action Indicated (NAI) · Nerviano

Key facts

Inspection ID 1072258
Firm NerPharMa S.r.l.
FEI number 3004762406
Address Bldgs 65 And 71 Casella Postale N. 11, Viale Luigi Pasteur 10
City Nerviano
Fiscal year 2019
Inspection end date Oct 26, 2018
Classification No Action Indicated (NAI)
Project area New Drug Evaluation
Product type Drugs

At a glance

  • None Citations
  • None 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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