FDA inspection

Kindeva Drug Delivery LP: FDA inspection ending Feb 20, 2001

FDA inspection 61795 · Voluntary Action Indicated (VAI) · Northridge, CA

Key facts

Inspection ID 61795
Firm Kindeva Drug Delivery LP
FEI number 2010441
Address 19901 Nordhoff St
City Northridge
State CA
ZIP 91324-3213
Fiscal year 2001
Inspection end date Feb 20, 2001
Classification Voluntary Action Indicated (VAI)
Project area New Drug Evaluation
Product type Drugs

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • Yes 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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