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Facility profile

Cambridge Isotope Laboratories, Inc.

Active pharmaceutical ingredient (API) manufacturing · Andover, MA

FDA recordFDA directory updated Jul 22, 2026Profile not yet claimed3 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.

Active pharmaceutical ingredient (API) manufacture
Due diligence

Regulatory record at a glance

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Registration record
Current FDA registration record

Expires Dec 31, 2026 · checked Jul 22, 2026

Latest matched inspection
No action indicated (NAI)

Jan 29, 2026 · No conditions warranted FDA action in this inspection.

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 no 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, Jun 2009 – Jan 2026 · 1 NAI · 6 VAI · 0 OAI

DateClassProject areaCitationsFY
Jan 29, 2026NAIDrug Quality Assurance2026
Aug 30, 2022VAIDrug Quality Assurance2022
Mar 25, 2016VAIDrug Quality Assurance2016
Mar 20, 2014VAIDrug Quality Assurance2014
Aug 22, 2011VAIDrug Quality Assurance2011
Feb 11, 2010VAIDrug Quality Assurance2010
Jun 18, 2009VAIDrug Quality Assurance2009

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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