Labverity
Facility profile

Grand River Aseptic Manufacturing, Inc.

Testing & analysis · Sterile processing · Grand Rapids, MI

FDA recordFDA directory updated Jul 21, 2026Profile not yet claimed4 registered company locations
Potential fit

Listed operations

The U.S. Food and Drug Administration (FDA) record lists broad activities for this site. Confirm specific services and availability directly.

AnalysisLabelPackSterilize
Due diligence

Regulatory record at a glance

Use these records to guide qualification; they are not a facility score.

Registration record
Current FDA registration record

Expires Dec 31, 2026 · checked Jul 21, 2026

Latest matched inspection
Voluntary action indicated (VAI)

Nov 4, 2025 · FDA documented observations for voluntary correction.

Matched compliance actions
None in our records

No warning letter, injunction, or seizure matched.

Understand this record

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Shows

Registration status and a latest matched voluntary action indicated inspection.

Doesn’t show

Exact services, availability, capacity, pricing, or overall quality.

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Method and source details
View full inspection and compliance history7 inspection records

FDA inspection history

7 records, Aug 2013 – Nov 2025 · 2 NAI · 5 VAI · 0 OAI

DateClassProject areaCitationsFY
Nov 4, 2025VAIDrug Quality AssuranceYes2026
Feb 21, 2024VAIVaccines and Allergenic Products2024
Jul 2, 2021VAIDrug Quality Assurance2021
Jun 20, 2018NAIDrug Quality Assurance2018
Dec 3, 2015NAIDrug Quality Assurance2016
Nov 24, 2014VAIDrug Quality AssuranceYes2015
Aug 28, 2013VAIDrug Quality Assurance2013

No action indicated (NAI) · Voluntary action indicated (VAI) · Official action indicated (OAI)

Matched compliance actions

No warning letter, injunction, or seizure is matched in the current data set.

Unclaimed profile

Service details not yet provided

Methods, equipment, quality scope, capacity, turnaround, and commercial contacts are not available.

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