FDA inspection

Wolff, Dr Ray: FDA inspection ending Oct 1, 1999

FDA inspection 926 · No Action Indicated (NAI) · Creve Coeur, MO

Key facts

Inspection ID 926
Firm Wolff, Dr Ray
FEI number 3002828239
Address 12401 Olive Blvd Ste 100
City Creve Coeur
State MO
ZIP 63141-5448
Fiscal year 2000
Inspection end date Oct 1, 1999
Classification No Action Indicated (NAI)
Project area Bio-Research Monit: Human Drugs
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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