Pots & Co Corporation

FDA Regulatory Profile

Pots & Co Corporation 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 "Pots & Co Corporation" and its spelling variants "Pots And Co Corporation", "Pots And Co".

Latest inspection
Jul 16, 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

Pots & Co Corporation's FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Pots & Co Corporation: FDA inspections per year 2017: 0 inspections020172018: 1 inspections120182019: 1 inspections120192020: 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
201910000
201810000
201700000

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 19, 2018 to Jul 16, 2024.

DateSiteProductClassificationFEI
Jul 16, 2024Los Angeles, CAFood/CosmeticsNo Action Indicated (NAI)3013782958
Aug 23, 2021Los Angeles, CAFood/CosmeticsNo Action Indicated (NAI)3013782958
Jul 11, 2019Mill Valley, CAFood/CosmeticsNo Action Indicated (NAI)3013433045
Oct 19, 2018London, United KingdomFood/CosmeticsVoluntary Action Indicated (VAI)3011683237

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means 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 3013782958Los Angeles, CA2Jul 16, 2024
FEI 3013433045Mill Valley, CA1Jul 11, 2019
FEI 3011683237London, United Kingdom1Oct 19, 2018

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