Dr. Paul Lohmann GmbH KG
FDA Inspections Database

Dr. Paul Lohmann GmbH KG

FDA Inspections Database

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

NAI · No Action Indicated Germany
  • Total Records 3
  • Latest Inspection 2016-04-14
  • Data Source U.S. FDA
  • Last Updated 2016-08-30
Company Overview

Company

Dr. Paul Lohmann GmbH KG

Country

Germany

Social Profiles

Company Snapshot

Dr. Paul Lohmann GmbH KG

Dr. Paul Lohmann GmbH KG | Hauptstrasse 2 | 31860 Emmerthal/Germany

Germany

www.lohmann4minerals.com/index.html sales@lohmann4minerals.com View on Map
FDA Inspections Timeline (3 records)
2016
14 Apr
No Action Indicated NAI

Legal Name

Dr. Paul Lohmann GmbH KG

Project Area

Drug Quality Assurance

Product Type

Drugs

Posted Citations

No

Inspection End Date

2016-04-14

FMD Date

2016-08-30

Fiscal Year

2016

State

Luneburg, Germany

Location

Luneburg, , Germany

Inspection Info

Fiscal Year: 2016
Citations: No

2012
23 Mar
No Action Indicated NAI

Legal Name

Dr. Paul Lohmann GmbH KG

Project Area

Food Composition, Standards, Labeling and Econ

Product Type

Food/Cosmetics

Posted Citations

No

Inspection End Date

2012-03-23

FMD Date

2012-05-29

Fiscal Year

2012

State

Emmerthal, Germany

Location

Emmerthal, , Germany

Inspection Info

Fiscal Year: 2012
Citations: No

2012
23 Mar
No Action Indicated NAI

Legal Name

Dr. Paul Lohmann GmbH KG

Project Area

Foodborne Biological Hazards

Product Type

Food/Cosmetics

Posted Citations

No

Inspection End Date

2012-03-23

FMD Date

2012-05-29

Fiscal Year

2012

State

Emmerthal, Germany

Location

Emmerthal, , Germany

Inspection Info

Fiscal Year: 2012
Citations: No

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Classification Breakdown
3 total
  • NAI (No 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

Luneburg, , Germany

Inspection Info

Fiscal Year: 2016
Citations: No

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

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