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Facility profile

Mannkind Corporation

Testing & analysis · Drug product manufacturing · Danbury, CT

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.

AnalysisLabelManufacturePack
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
No action indicated (NAI)

Nov 4, 2025 · No conditions warranted FDA action in this inspection.

Matched compliance actions
Past action on file · 2018

More than five years old · review later records.

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Shows

Registration status and a latest matched no action indicated inspection.

Doesn’t show

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

FDA inspection history

7 records, Dec 2009 – Nov 2025 · 4 NAI · 3 VAI · 0 OAI

DateClassProject areaCitationsFY
Nov 4, 2025NAIDrug Quality Assurance2026
Aug 6, 2021VAIDrug Quality Assurance2021
Jun 19, 2018NAIDrug Quality Assurance2018
Jun 19, 2018NAICompliance: Devices2018
May 17, 2013VAIDrug Quality AssuranceYes2013
Dec 4, 2009VAIDrug Quality Assurance2010
Dec 4, 2009NAICompliance: Devices2010

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

Matched compliance actions

Oct 5, 2018Warning Letter · CDER
Unclaimed profile

Service details not yet provided

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

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