FDA inspection

Purolite S.R.L.: FDA inspection ending Feb 19, 2004

FDA inspection 317643 · No Action Indicated (NAI) · Victoria

Key facts

Inspection ID 317643
Firm Purolite S.R.L.
FEI number 3004201705
Address Str. Aleea Uzinei Nr. 11
City Victoria
Fiscal year 2004
Inspection end date Feb 19, 2004
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
  • 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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