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Facility profile

Noramco, LLC

Active pharmaceutical ingredient (API) manufacturing · Wilmington, DE

FDA recordFDA directory updated Jul 22, 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) manufactureParticle Size ReductionRepack
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 22, 2026

Latest matched inspection
Voluntary action indicated (VAI)

Oct 15, 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 history8 inspection records

FDA inspection history

8 records, Aug 2010 – Oct 2025 · 5 NAI · 3 VAI · 0 OAI

DateClassProject areaCitationsFY
Oct 15, 2025VAIDrug Quality Assurance2026
Nov 18, 2022NAIDrug Quality Assurance2023
Feb 21, 2019NAIDrug Quality Assurance2019
Nov 17, 2017VAIDrug Quality Assurance2018
Jan 21, 2016NAIDrug Quality Assurance2016
Nov 13, 2014NAIDrug Quality Assurance2015
Apr 27, 2012NAIDrug Quality Assurance2012
Aug 2, 2010VAIDrug Quality Assurance2010

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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