Horst Schluckwerder OHG

FDA Regulatory Profile

Horst Schluckwerder OHG has 0 FDA recalls, 2 inspections, 0 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "Horst Schluckwerder OHG".

Latest inspection
Dec 13, 2018 · NAI

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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 13, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA inspections

2 inspections on Dec 13, 2018.

DateSiteProductClassificationFEI
Dec 13, 2018Adendorf, GermanyFood/CosmeticsNo Action Indicated (NAI)3014699866
Dec 13, 2018Adendorf, GermanyFood/CosmeticsNo Action Indicated (NAI)3005130009
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 3005130009Adendorf, Germany1Dec 13, 2018
FEI 3014699866Adendorf, Germany1Dec 13, 2018

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