J.M. Huber Micropowders, Inc. FDA Record

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

J.M. Huber Micropowders, Inc. has 0 FDA recalls, 11 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "J.M. Huber Micropowders, Inc." is on file.

What these totals cover: FDA records filed under the name "J.M. Huber Micropowders, Inc." and its spelling variant "J.M. Huber Micropowders".

Latest inspection
Jun 2, 2026 · 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
Inspections11Nov 14, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

FDA record by year

J.M. Huber Micropowders, Inc.'s FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

J.M. Huber Micropowders, Inc.: FDA inspections per year 2017: 2 inspections220172018: 1 inspections120182019: 0 inspections020192020: 0 inspections020202021: 2 inspections220212022: 0 inspections020222023: 0 inspections020232024: 0 inspections020242025: 1 inspections120252026: 2 inspections22026
YearInspectionsOAIWarning lettersRecall recordsClass I
202620000
202511000
202400000
202300000
202200000
202120000
202000000
201900000
201811000
201720000

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

11 inspections from Jan 18, 2012 to Jun 2, 2026.

DateSiteProductClassificationFEI
Jun 2, 2026Quincy, ILFood/CosmeticsNo Action Indicated (NAI)3015047058
Feb 11, 2026La Mirada, CADrugsVoluntary Action Indicated (VAI)3003665718
Dec 5, 2025Quincy, ILDrugsOfficial Action Indicated (OAI)3002981536
Aug 27, 2021Quincy, ILDrugsVoluntary Action Indicated (VAI)3002981536
Jun 25, 2021La Mirada, CADrugsVoluntary Action Indicated (VAI)3003665718
Aug 10, 2018Quincy, ILVeterinaryOfficial Action Indicated (OAI)3002981536
Oct 23, 2017La Mirada, CAFood/CosmeticsNo Action Indicated (NAI)3003665718
Sep 12, 2017Quincy, ILVeterinaryNo Action Indicated (NAI)3002981536
Dec 17, 2014Quincy, ILDrugsVoluntary Action Indicated (VAI)3002981536
Oct 30, 2014La Mirada, CAFood/CosmeticsNo Action Indicated (NAI)3003665718
Jan 18, 2012La Mirada, CAFood/CosmeticsVoluntary Action Indicated (VAI)3003665718
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 3015047058Quincy, IL1Jun 2, 2026
FEI 3003665718La Mirada, CA5Feb 11, 2026
FEI 3002981536Quincy, IL5Dec 5, 2025

J.M. Huber Micropowders, Inc. and the FDA: common questions

Has J.M. Huber Micropowders, Inc. received an FDA warning letter?

No FDA warning letter addressed to the name "J.M. Huber Micropowders, Inc." 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 J.M. Huber Micropowders, Inc. received an FDA Form 483?

FDA has not published a Form 483 for "J.M. Huber Micropowders, Inc." in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect J.M. Huber Micropowders, Inc.?

The most recent FDA inspection on file ended Jun 2, 2026 at Quincy, IL and was classified NAI. FDA has 11 inspections of J.M. Huber Micropowders, Inc. on file, 2 of them classified OAI (official action indicated).

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