Dr. Paul Lohmann GmbH KG FDA Record

Warning letters, Form 483s, inspections, recalls and 510(k) clearances

Dr. Paul Lohmann GmbH KG has 0 FDA recalls, 2 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Dr. Paul Lohmann GmbH KG" is on file.

What these totals cover: FDA records filed under the name "Dr. Paul Lohmann GmbH KG" and its spelling variant "Paul Lohmann Gmbh Kg". Records filed under related names are not included; see Related names.

Latest inspection
Apr 14, 2016 · NAI

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections2Nov 14, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

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Recent FDA inspections

2 inspections from Mar 23, 2012 to Apr 14, 2016.

DateSiteProductClassificationFEI
Apr 14, 2016Luneburg, GermanyDrugsNo Action Indicated (NAI)3004273210
Mar 23, 2012Emmerthal, GermanyFood/CosmeticsNo Action Indicated (NAI)3004273201
NAI
No objectionable conditions or practices were found during the inspection.
VAI
Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
OAI
Regulatory and/or administrative actions are recommended.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

FDA-inspected facilities

2 inspected sites, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3004273210Luneburg, Germany1Apr 14, 2016
FEI 3004273201Emmerthal, Germany1Mar 23, 2012

Dr. Paul Lohmann GmbH KG and the FDA: common questions

Has Dr. Paul Lohmann GmbH KG received an FDA warning letter?

No FDA warning letter addressed to the name "Dr. Paul Lohmann GmbH KG" is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.

Has Dr. Paul Lohmann GmbH KG received an FDA Form 483?

FDA has not published a Form 483 for "Dr. Paul Lohmann GmbH KG" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Dr. Paul Lohmann GmbH KG?

The most recent FDA inspection on file ended Apr 14, 2016 at Luneburg, Germany and was classified NAI. FDA has 2 inspections of Dr. Paul Lohmann GmbH KG on file.

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Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.