FDA inspection

Knoll Pharmaceutical Company: FDA inspection ending Jan 28, 2000

FDA inspection 8942 · Voluntary Action Indicated (VAI) · Budd Lake, NJ

Key facts

Inspection ID 8942
Firm Knoll Pharmaceutical Company
FEI number 3002854688
Address 3000 Continental Dr N
City Budd Lake
State NJ
ZIP 07828-1202
Fiscal year 2000
Inspection end date Jan 28, 2000
Classification Voluntary Action Indicated (VAI)
Project area Post Mrkt Surv & Epid: Human Drugs
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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