FDA inspection

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

FDA inspection 1293366 · Voluntary Action Indicated (VAI) · Caledonia, MI

Key facts

Inspection ID 1293366
Firm Grand River Aseptic Manufacturing Inc.
FEI number 3019594046
Address 6670 Patterson Ave Se Ste 1a
City Caledonia
State MI
ZIP 49316
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
  • 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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