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Facility profile

Shandong Lukang Shelile Pharmaceutical Co., Ltd.

Active pharmaceutical ingredient (API) manufacturing · Shandong 273500 · China

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

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
No action indicated (NAI)

Apr 30, 2026 · No conditions warranted FDA action in this inspection.

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 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, Jul 2009 – Apr 2026 · 7 NAI · 2 VAI · 0 OAI

DateClassProject areaCitationsFY
Apr 30, 2026NAIPre-Approval Eval. of Animal Drugs and Food Additives2026
May 30, 2025VAIMonitoring of Marketed Animal Drugs, Feed, and Devices2025
Dec 14, 2018NAIDrug Quality Assurance2019
Dec 14, 2018NAIMonitoring of Marketed Animal Drugs, Feed, and Devices2019
Nov 6, 2015NAIMonitoring of Marketed Animal Drugs, Feed, and Devices2016
Dec 5, 2013NAIPre-Approval Eval. of Animal Drugs and Food Additives2014
Dec 5, 2013NAIMonitoring of Marketed Animal Drugs, Feed, and Devices2014
Dec 5, 2013NAIDrug Quality Assurance2014
Jul 30, 2009VAIPre-Approval Eval. of Animal Drugs and Food Additives2009

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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