August Storck KG FDA Record

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

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

What these totals cover: FDA records filed under the name "August Storck KG". Records filed under related names are not included; see Related names.

Latest inspection
Mar 29, 2019 · 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

FDA record by year

August Storck KG's FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

August Storck KG: FDA inspections per year 2017: 1 inspections120172018: 0 inspections020182019: 1 inspections120192020: 0 inspections020202021: 0 inspections020212022: 0 inspections020222023: 0 inspections020232024: 0 inspections020242025: 0 inspections020252026: 0 inspections02026
YearInspectionsOAIWarning lettersRecall recordsClass I
202600000
202500000
202400000
202300000
202200000
202100000
202000000
201910000
201800000
201710000

Inspections are counted by the date they ended, warning letters by the date FDA issued them and recall records by the recall start date. FDA lists one recall record per recalled product, so one recall event can add several.

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Recent FDA inspections

2 inspections from Jan 24, 2017 to Mar 29, 2019.

DateSiteProductClassificationFEI
Mar 29, 2019Ohrdruf, GermanyFood/CosmeticsNo Action Indicated (NAI)3004319292
Jan 24, 2017Berlin, GermanyFood/CosmeticsVoluntary Action Indicated (VAI)3004318632
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 3004319292Ohrdruf, Germany1Mar 29, 2019
FEI 3004318632Berlin, Germany1Jan 24, 2017

August Storck KG and the FDA: common questions

Has August Storck KG received an FDA warning letter?

No FDA warning letter addressed to the name "August Storck 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 August Storck KG received an FDA Form 483?

FDA has not published a Form 483 for "August Storck KG" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect August Storck KG?

The most recent FDA inspection on file ended Mar 29, 2019 at Ohrdruf, Germany and was classified NAI. FDA has 2 inspections of August Storck KG on file.

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