FDA inspection

Astellas Pharma Manufacturing, Inc.: FDA inspection ending Aug 24, 2005

FDA inspection 392375 · No Action Indicated (NAI) · Grand Island, NY

Key facts

Inspection ID 392375
Firm Astellas Pharma Manufacturing, Inc.
FEI number 1317274
Address 3125 Staley Rd
City Grand Island
State NY
ZIP 14072-2028
Fiscal year 2005
Inspection end date Aug 24, 2005
Classification No Action Indicated (NAI)
Project area Drug Quality Assurance
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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