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Charbonnel Et Walker Ltd

FDA Regulatory Profile

Charbonnel Et Walker Ltd has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "Charbonnel Et Walker Ltd" and its spelling variants "Charbonnel Et Walker", "Charbonnel Et Walker Limited".

Latest inspection
Apr 12, 2024 · 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
Inspections4Nov 13, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

FDA record by year

Charbonnel Et Walker Ltd's FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Charbonnel Et Walker Ltd: FDA inspections per year 2017: 1 inspections120172018: 0 inspections020182019: 0 inspections020192020: 0 inspections020202021: 1 inspections120212022: 0 inspections020222023: 0 inspections020232024: 1 inspections120242025: 0 inspections020252026: 0 inspections02026
YearInspectionsOAIWarning lettersRecall recordsClass I
202600000
202500000
202410000
202300000
202200000
202110000
202000000
201900000
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.

Recent FDA inspections

4 inspections from Oct 18, 2011 to Apr 12, 2024.

DateSiteProductClassificationFEI
Apr 12, 2024New Braunfels, TXFood/CosmeticsNo Action Indicated (NAI)3014782307
Sep 1, 2021New Braunfels, TXFood/CosmeticsNo Action Indicated (NAI)3014782307
Jun 22, 2017Dorchester, United KingdomFood/CosmeticsNo Action Indicated (NAI)3004279472
Oct 18, 2011Tunbridge Wells, United KingdomFood/CosmeticsNo Action Indicated (NAI)3001634687
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

3 inspected sites, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3014782307New Braunfels, TX2Apr 12, 2024
FEI 3004279472Dorchester, United Kingdom1Jun 22, 2017
FEI 3001634687Tunbridge Wells, United Kingdom1Oct 18, 2011

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FDA data resources

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