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Facility profile

Frontida BioPharm, LLC

Testing & analysis · Drug product manufacturing · Philadelphia, PA

FDA recordFDA directory updated Jul 21, 2026Profile not yet claimed2 registered company locations
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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
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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)

Apr 2, 2026 · No conditions warranted FDA action in this inspection.

Matched compliance actions
Past action on file · 2016

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 history11 inspection records

FDA inspection history

11 records, Dec 2008 – Apr 2026 · 4 NAI · 6 VAI · 1 OAI

DateClassProject areaCitationsFY
Apr 2, 2026NAIDrug Quality Assurance2026
Jul 22, 2025NAITobacco Post-Market Activities2025
Dec 7, 2023VAIDrug Quality Assurance2024
Jul 19, 2019VAIDrug Quality AssuranceYes2019
Mar 31, 2017VAIDrug Quality AssuranceYes2017
Jul 17, 2015OAIDrug Quality AssuranceYes2015
Jul 25, 2014VAIDrug Quality Assurance2014
Jan 27, 2012VAIDrug Quality Assurance2012
May 20, 2011VAIDrug Quality Assurance2011
Jun 30, 2009NAIBioresearch Monitoring2009
Dec 10, 2008NAIDrug Quality Assurance2009

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

Matched compliance actions

Aug 15, 2016Warning Letter · CDER
Unclaimed profile

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