FDA inspection

Archimica S.p.A: FDA inspection ending Sep 13, 2018

FDA inspection 1123733 · Voluntary Action Indicated (VAI) · Lodi

Key facts

Inspection ID 1123733
Firm Archimica S.p.A
FEI number 3002874947
Address Viale Milano 86
City Lodi
Country Italy
Fiscal year 2018
Inspection end date Sep 13, 2018
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • None 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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