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AMPAC Fine Chemicals LLC

Testing & analysis · Active pharmaceutical ingredient (API) manufacturing · RANCHO CORDOVA, CA

FDA recordFDA directory updated Jul 21, 2026Profile not yet claimed3 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.

AnalysisActive 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 21, 2026

Latest matched inspection
No action indicated (NAI)

Sep 10, 2025 · No conditions warranted FDA action in this inspection.

Matched compliance actions
Past action on file · 2010

More than five years old · review later records.

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Shows

Registration status and a latest matched no action indicated inspection.

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Method and source details
View full inspection and compliance history9 inspection records

FDA inspection history

9 records, Feb 2010 – Sep 2025 · 2 NAI · 6 VAI · 1 OAI

DateClassProject areaCitationsFY
Sep 10, 2025NAIDrug Quality Assurance2025
Jan 31, 2019NAIDrug Quality Assurance2019
Nov 8, 2016VAIDrug Quality Assurance2017
Jan 23, 2015VAIDrug Quality Assurance2015
Dec 13, 2012VAIDrug Quality Assurance2013
Apr 20, 2012VAIDrug Quality Assurance2012
Aug 12, 2011VAIDrug Quality Assurance2011
Mar 4, 2011VAIDrug Quality Assurance2011
Feb 19, 2010OAIDrug Quality Assurance2010

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

Matched compliance actions

Jul 1, 2010Warning Letter · CDER
Unclaimed profile

Service details not yet provided

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