FDA inspection

Grand River Aseptic Manufacturing, Inc.: FDA inspection ending Nov 4, 2025

FDA inspection 1293364 · Voluntary Action Indicated (VAI) · Grand Rapids, MI

Key facts

Inspection ID 1293364
Firm Grand River Aseptic Manufacturing, Inc.
FEI number 3008716173
Address 140 Front Ave Sw Ste 3
City Grand Rapids
State MI
ZIP 49504
Country United States
Fiscal year 2026
Inspection end date Nov 4, 2025
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No 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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