Herbstreith & Fox KG Pektin-Fabriken FDA Record

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

  • Latest inspection NAI · Jun 8, 2018
  • No warning letters matched by name
Inspections 1 0 OAI
Recalls 0 0 Class I
Warning letters 0 None on file
510(k) clearances 0 None on file

Herbstreith & Fox KG Pektin-Fabriken has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Herbstreith & Fox KG Pektin-Fabriken" is on file.

What these totals cover: FDA records filed under the name "Herbstreith & Fox KG Pektin-Fabriken" and its spelling variant "Herbstreith And Fox Kg Pektin-Fabriken".

Latest inspection
Jun 8, 2018 · 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
Inspections1Nov 14, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

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Recent FDA inspections

1 inspection on Jun 8, 2018.

DateSiteProductClassificationFEI
Jun 8, 2018Neuenburg, GermanyFood/CosmeticsNo Action Indicated (NAI)3003101258
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.

FacilityLocationInspectionsLatest
FEI 3003101258Neuenburg, Germany1Jun 8, 2018

Herbstreith & Fox KG Pektin-Fabriken and the FDA: common questions

Has Herbstreith & Fox KG Pektin-Fabriken received an FDA warning letter?

No FDA warning letter addressed to the name "Herbstreith & Fox KG Pektin-Fabriken" 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 Herbstreith & Fox KG Pektin-Fabriken received an FDA Form 483?

FDA has not published a Form 483 for "Herbstreith & Fox KG Pektin-Fabriken" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Herbstreith & Fox KG Pektin-Fabriken?

The most recent FDA inspection on file ended Jun 8, 2018 at Neuenburg, Germany and was classified NAI. FDA has 1 inspection of Herbstreith & Fox KG Pektin-Fabriken on file.

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