LGM Pharma - OAI
FDA Inspections Database

LGM Pharma - OAI

FDA Inspections Database

U.S. FDA inspection classifications and citation records from the official FDA inspection database.

OAI · Official Action Indicated United States
  • Total Records 3
  • Latest Inspection 2022-04-08
  • Data Source U.S. FDA
  • Last Updated -

4

All
View

1

VAI
View

3

OAI
View
Company Overview

Company

LGM Pharma - OAI

Country

U.S.A

Social Profiles

LinkedIn X / Twitter
Company Snapshot

LGM Pharma - OAI

6400 Congress Avenue, Suite 1400 Boca Raton, FL 33487

U.S.A

lgmpharma.com/ info@lgmpharma.com View on Map
FDA Inspections Timeline (3 records)
2022
08 Apr
Official Action Indicated OAI

Legal Name

LGM Pharma LLC

Project Area

Drug Quality Assurance

Product Type

Drugs

Posted Citations

No

Inspection End Date

2022-04-08

FMD Date

-

Fiscal Year

2022

State

Kentucky

Erlanger, United States

Location

Erlanger, Kentucky, United States

Inspection Info

Fiscal Year: 2022
Citations: No

2022
08 Apr
Official Action Indicated OAI

Legal Name

LGM Pharma LLC

Project Area

Monitoring of Marketed Animal Drugs, Feed, and Devices

Product Type

Veterinary

Posted Citations

No

Inspection End Date

2022-04-08

FMD Date

-

Fiscal Year

2022

State

Kentucky

Erlanger, United States

Location

Erlanger, Kentucky, United States

Inspection Info

Fiscal Year: 2022
Citations: No

2018
04 Dec
Official Action Indicated OAI

Legal Name

LGM Pharma LLC

Project Area

Drug Quality Assurance

Product Type

Drugs

Posted Citations

No

Inspection End Date

2018-12-04

FMD Date

-

Fiscal Year

2019

State

Kentucky

Erlanger, United States

Location

Erlanger, Kentucky, United States

Inspection Info

Fiscal Year: 2019
Citations: No

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Classification Breakdown
3 total
  • OAI (Official Action Indicated)
Official Source

All data is sourced from the official FDA inspection database maintained by the U.S. Food and Drug Administration.

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Location

Erlanger, Kentucky, United States

Inspection Info

Fiscal Year: 2022
Citations: No

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FDA inspection data is compiled from publicly available U.S. FDA inspection classification records.

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