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Sonneborn, LLC

Active pharmaceutical ingredient (API) manufacturing · Petrolia, PA

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

Latest matched inspection
Voluntary action indicated (VAI)

Aug 20, 2025 · FDA documented observations for voluntary correction.

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 voluntary 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 history9 inspection records

FDA inspection history

9 records, May 2009 – Aug 2025 · 8 NAI · 1 VAI · 0 OAI

DateClassProject areaCitationsFY
Aug 20, 2025VAIDrug Quality AssuranceYes2025
Nov 1, 2021NAIFoodborne Biological Hazards2022
Jul 10, 2019NAIDrug Quality Assurance2019
Sep 12, 2018NAIFoodborne Biological Hazards2018
Sep 12, 2018NAIFood Composition, Standards, Labeling and Econ2018
Jun 30, 2014NAIFoodborne Biological Hazards2014
Jun 30, 2014NAIDrug Quality Assurance2014
Jun 24, 2010NAIDrug Quality Assurance2010
May 28, 2009NAIDrug 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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