Labverity
Facility profile

Thatcher Company

Drug product manufacturing · Active pharmaceutical ingredient (API) manufacturing · Salt Lake City, UT

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) manufactureManufacture
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 17, 2025 · 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.

Doesn’t show

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

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

FDA inspection history

7 records, Aug 2011 – Sep 2025 · 4 NAI · 3 VAI · 0 OAI

DateClassProject areaCitationsFY
Sep 17, 2025NAIMonitoring of Marketed Animal Drugs, Feed, and Devices2025
Sep 17, 2025NAIDrug Quality Assurance2025
Oct 23, 2019NAIDrug Quality Assurance2020
Sep 18, 2018VAIDrug Quality AssuranceYes2018
Dec 10, 2015VAIDrug Quality AssuranceYes2016
May 24, 2012NAIDrug Quality Assurance2012
Aug 12, 2011VAIDrug Quality Assurance2011

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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