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Facility profile

Vericel Corporation

Testing & analysis · Drug product manufacturing · Cambridge, MA

FDA recordFDA directory updated Jul 21, 2026Profile not yet claimed
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Listed operations

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

AnalysisActive pharmaceutical ingredient (API) manufactureLabelManufacturePack
Due diligence

Regulatory record at a glance

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Registration record
Current FDA registration record

Expires Dec 31, 2026 · checked Jul 21, 2026

Latest matched inspection
Voluntary action indicated (VAI)

Sep 25, 2024 · FDA documented observations for voluntary correction.

Matched compliance actions
None in our records

No warning letter, injunction, or seizure matched.

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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 history8 inspection records

FDA inspection history

8 records, Aug 2009 – Sep 2024 · 1 NAI · 7 VAI · 0 OAI

DateClassProject areaCitationsFY
Sep 25, 2024VAICompliance: DevicesYes2024
Sep 25, 2024VAIPostmarket Assurance: DevicesYes2024
Jul 21, 2023NAICompliance: DevicesYes2023
Jul 21, 2023VAIHuman Cellular, Tissue, and Gene TherapiesYes2023
May 27, 2016VAIHuman Cellular, Tissue, and Gene Therapies2016
Mar 19, 2014VAIHuman Cellular, Tissue, and Gene Therapies2014
Sep 27, 2011VAIHuman Cellular, Tissue, and Gene Therapies2011
Aug 21, 2009VAIHuman Cellular, Tissue, and Gene TherapiesYes2009

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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