Labverity
Facility profile

ChemPacific Corporation

Active pharmaceutical ingredient (API) manufacturing · Baltimore, MD

FDA recordFDA directory updated Jul 21, 2026Profile not yet claimed2 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

Use these records to guide qualification; they are not a facility score.

Registration record
Current FDA registration record

Expires Dec 31, 2026 · checked Jul 21, 2026

Latest matched inspection
Voluntary action indicated (VAI)

Apr 7, 2026 · FDA documented observations for voluntary correction.

Matched compliance actions
Past action on file · 2011

More than five years old · review later records.

Understand this record

Use the evidence, then ask for fit.

Shows

Registration status and a latest matched voluntary action indicated inspection.

Doesn’t show

Exact services, availability, capacity, pricing, or overall quality.

Ask next

Ask what was corrected and review any later inspection or follow-up record.

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

FDA inspection history

7 records, Feb 2010 – Apr 2026 · 2 NAI · 3 VAI · 2 OAI

DateClassProject areaCitationsFY
Apr 7, 2026VAIDrug Quality Assurance2026
Feb 15, 2024VAIDrug Quality Assurance2024
Aug 18, 2016NAIDrug Quality Assurance2016
Apr 9, 2013NAIDrug Quality Assurance2013
Nov 18, 2011VAIDrug Quality Assurance2012
Oct 14, 2010OAIDrug Quality Assurance2011
Feb 17, 2010OAIDrug Quality Assurance2010

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

Matched compliance actions

Apr 7, 2011Warning Letter · CDER
Unclaimed profile

Service details not yet provided

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

Ask about services