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Finemost Corporation FDA Inspection Record

FEI 3003253809 · Inspections, Form 483s, warning letters and import refusals

Finemost Corporation is an FDA-inspected facility (FEI 3003253809) located in Cerritos, CA, US. RegDataLab tracks 8 FDA inspections and 1 compliance action at this facility.

What FDA found at this site

Latest inspection
Jul 26, 2018: Voluntary Action Indicated (VAI)
Inspections on record
8 (1 OAI, 6 VAI, 1 NAI)
Last OAI inspection
Sep 21, 2012
Warning letters
1 listed by FDA for this FEI, latest Mar 20, 2013
Recalls as the recalling firm
1, latest Jul 28, 2011

A Form 483 lists an inspector's observations. OAI means FDA recommends regulatory and/or administrative action. A warning letter is FDA's formal enforcement notice. No record here does not establish that a site is safe. Check this site on FDA's Data Dashboard.

Inspections and what FDA cited

Newest first. Citations are the inspector observations FDA publishes for the inspection.

DateResultWhat FDA cited
Jul 26, 2018Voluntary Action Indicated (VAI)Testing and release for distribution (21 CFR 211.165(a))
Nov 14, 2017Voluntary Action Indicated (VAI)Equipment - maintain, clean, sanitize (21 CFR 111.27(d))
Specifications met, in-process - quality finished batch (21 CFR 111.75(b)(1))
Aug 26, 2016Voluntary Action Indicated (VAI)No citations listed
Aug 10, 2015Voluntary Action Indicated (VAI)Batch record - follow master (21 CFR 111.255(c))
Batch record - date, time; maintenance (21 CFR 111.260(c))
Standard reference materials; criteria for selecting (21 CFR 111.315(d))
Component - verify identity, dietary ingredient (21 CFR 111.75(a)(1)(i))
and 2 more
Feb 28, 2014Voluntary Action Indicated (VAI)Batch record - complete (21 CFR 111.255(b))
Master manufacturing record - specifications; quality (21 CFR 111.205(b)(1))
Specifications-component purity, strength, composition (21 CFR 111.70(b)(2))
Specifications - contamination limits (21 CFR 111.70(b)(3))
and 4 more
Sep 21, 2012Official Action Indicated (OAI)Personnel - quality control personnel - qualified (21 CFR 111.12)
Batch record - complete (21 CFR 111.255(b))
Master manufacturing record - specifications; quality (21 CFR 111.205(b)(1))
Specifications - identity, purity, strength, composition (21 CFR 111.70(e))
and 3 more
Apr 19, 2011No Action Indicated (NAI)Written procedures - sick or infected personnel (21 CFR 111.8)
Personnel - records - training (21 CFR 111.14(b)(2))
Records - cleaning, pest control (21 CFR 111.23(b))
Procedures - calibrating automated, mechanical equip (21 CFR 111.25(b))
and 7 more
Mar 19, 2010Voluntary Action Indicated (VAI)Lack of Written MDR Procedures (21 CFR 803.17)

Recalls

Newest first. Recalls FDA's Enforcement Report lists with this FEI as the recalling firm. The recalling firm is not always the site that made the product. Search FDA's Enforcement Report by recall number.

DateClassRecallProduct and reason
Jul 28, 2011Class IF-0375-2012Shi Shen Tang Mahuang & Cimicifuga Combination; Item # 20217; Mfg No. CP10217, Use By… and 2 more products
The recall was initiated because Finemost Corporation dba Qualiherb confirmed that Shi Shen Tang, Shen Mi Tang, Xu Ming Tang, and Ding Chuan…

FDA record score

3 of 100. A count of this site's adverse public FDA records, weighted by how recent each one is. A higher number means more, or more recent, records. Each record below adds the points shown.

Counted on Nov 15, 2026, method version 1. It counts records and does not judge the site: a low number does not establish that a site is safe, and sites that FDA inspects more often can collect more points. How this is counted.

9 records behind this number
RecordDatePoints x age weightAdds
Inspection classified VAIJul 26, 20186 x 0.251.5
Inspection classified VAINov 14, 20176 x 0.251.5
Inspection classified VAIAug 26, 201610 years or older, so it adds no points0
Inspection classified VAIAug 10, 201510 years or older, so it adds no points0
Inspection classified VAIFeb 28, 201410 years or older, so it adds no points0
Warning letter on FDA's dashboard, which does not show close-outsMar 20, 201310 years or older, so it adds no points0
Inspection classified OAISep 21, 201210 years or older, so it adds no points0
Class I recall F-0375-2012, this FEI as the recalling firmJul 28, 201110 years or older, so it adds no points0
Inspection classified VAIMar 19, 201010 years or older, so it adds no points0

When each source was last refreshed

FDA sources behind this page and when RegDataLab last refreshed each one
RecordsLast refreshedSource as ofStatus
InspectionsNov 14, 2026Newest record Nov 5, 2026Current
Inspection citationsNov 14, 2026Newest record Nov 5, 2026Current
Compliance actions (warning letters, injunctions and other action types)Nov 2, 2026Newest record Oct 29, 2026Current
Warning letter textNov 14, 2026Newest record Nov 10, 2026Current
Recalls (Enforcement Report)Nov 14, 2026Newest record Nov 11, 2026Current
Form 483s and inspection documentsNov 13, 2026Newest record Nov 12, 2026Current
Import refusalsNov 2, 2026Newest record Oct 22, 2026Current

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Facility details

Company
Finemost Corporation
Location
Cerritos, CA (US)
Source
inspections

Compliance actions

FDA data resources

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