FDA inspection

Grand River Aseptic Manufacturing Inc.: FDA inspection ending Feb 21, 2024

FDA inspection 1236900 · No Action Indicated (NAI) · Caledonia, MI

Key facts

Inspection ID 1236900
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 2024
Inspection end date Feb 21, 2024
Classification No Action Indicated (NAI)
Project area Vaccines and Allergenic Products
Product type Biologics

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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