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Henry Lambertz GmbH & Co. KG FDA Record

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

Henry Lambertz GmbH & Co. KG has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Henry Lambertz GmbH & Co. KG" is on file.

What these totals cover: FDA records filed under the name "Henry Lambertz GmbH & Co. KG" and its spelling variant "Henry Lambertz Gmbh And Co. Kg". Records filed under related names are not included; see Related names.

Latest inspection: Sep 19, 2018 · NAI

Summary

Record counts and when each FDA source was last refreshed
Records	Count	Last refreshed	Source as of	Status
Recalls	0	Nov 8, 2026	File dated Nov 3, 2026	Current
510(k) clearances	0	Nov 8, 2026	File dated Nov 2, 2026	Current
Inspections	1	Nov 14, 2026	Newest record Nov 5, 2026	Current
Compliance actions	0	Nov 2, 2026	Newest record Oct 29, 2026	Current

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Related names

Each name below has its own page. Its counts cover only the records FDA filed under that name and are not part of the totals for Henry Lambertz GmbH & Co. KG above.

Name	Relation	Recalls	510(k)	Inspections	Compliance actions	Most recent recall
Henry Lambertz	Same company group	0	0	2	0	—

Recent FDA inspections

1 inspection on Sep 19, 2018.

Date	Site	Product	Classification	FEI
Sep 19, 2018	Aachen, Germany	Food/Cosmetics	No Action Indicated (NAI)	1000238545

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

1 inspected site, newest inspection first.

Facility	Location	Inspections	Latest
FEI 1000238545	Aachen, Germany	1	Sep 19, 2018

Henry Lambertz GmbH & Co. KG and the FDA: common questions

Has Henry Lambertz GmbH & Co. KG received an FDA warning letter?

No FDA warning letter addressed to the name "Henry Lambertz GmbH & Co. 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 Henry Lambertz GmbH & Co. KG received an FDA Form 483?

FDA has not published a Form 483 for "Henry Lambertz GmbH & Co. KG" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Henry Lambertz GmbH & Co. KG?

The most recent FDA inspection on file ended Sep 19, 2018 at Aachen, Germany and was classified NAI. FDA has 1 inspection of Henry Lambertz GmbH & Co. KG on file.

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