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Heinrich Klenk Gmbh FDA Record

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

Latest inspection NAI · Dec 12, 2018
No warning letters matched by name

Inspections 2

0 OAI

Recalls 0 0 Class I

Warning letters 0 None on file

510(k) clearances 0 None on file

Heinrich Klenk Gmbh has 0 FDA recalls, 2 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Heinrich Klenk Gmbh" is on file.

What these totals cover: FDA records filed under the name "Heinrich Klenk Gmbh" and its spelling variant "Heinrich Klenk". Records filed under related names are not included; see Related names.

Latest inspection: Dec 12, 2018 · NAI

Summary

Record counts and when each FDA source was last refreshed
Records	Count	Last refreshed	Source as of	Status
Recalls	0	Nov 11, 2026 (checked Nov 15, 2026, unchanged)	File dated Nov 10, 2026	Current
510(k) clearances	0	Nov 15, 2026	File dated Nov 9, 2026	Current
Inspections	2	Nov 15, 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 Heinrich Klenk Gmbh above.

Name	Relation	Recalls	510(k)	Inspections	Compliance actions	Most recent recall
Heinrich Klenk Gmbh And Co Kg	Same company group	0	0	2	0	—

Recent FDA inspections

2 inspections from Mar 27, 2012 to Dec 12, 2018.

Date	Site	Product	Classification	FEI
Dec 12, 2018	Schwebheim, Germany	Food/Cosmetics	No Action Indicated (NAI)	1000379630
Mar 27, 2012	Schwebheim, Germany	Food/Cosmetics	Voluntary Action Indicated (VAI)	1000379630

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 1000379630	Schwebheim, Germany	2	Dec 12, 2018

Heinrich Klenk Gmbh and the FDA: common questions

Has Heinrich Klenk Gmbh received an FDA warning letter?

No FDA warning letter addressed to the name "Heinrich Klenk Gmbh" 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 Heinrich Klenk Gmbh received an FDA Form 483?

FDA has not published a Form 483 for "Heinrich Klenk Gmbh" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Heinrich Klenk Gmbh?

The most recent FDA inspection on file ended Dec 12, 2018 at Schwebheim, Germany and was classified NAI. FDA has 2 inspections of Heinrich Klenk Gmbh on file.

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