CMI Cosmetic Manufacturers Inc. FDA Record

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

  • Latest inspection OAI · Oct 24, 2012
  • Last warning letter 2013
Inspections 1 1 OAI
Recalls 0 0 Class I
Warning letters 1 Latest Apr 25, 2013
510(k) clearances 0 None on file

CMI Cosmetic Manufacturers Inc. has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 1 compliance action on record. FDA has issued 1 warning letter to CMI Cosmetic Manufacturers Inc., the most recent on Apr 25, 2013.

What these totals cover: FDA records filed under the name "CMI Cosmetic Manufacturers Inc." and its spelling variant "Cmi Cosmetic Manufacturers".

Latest inspection
Oct 24, 2012 · OAI

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 11, 2026 (checked Nov 15, 2026, unchanged)File dated Nov 10, 2026Current
510(k) clearances0Nov 15, 2026File dated Nov 9, 2026Current
Inspections1Nov 15, 2026Newest record Nov 5, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Reviewing CMI Cosmetic Manufacturers Inc. as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.

Check this supplier

Or check CMI Cosmetic Manufacturers Inc. yourself in Claude, Cursor or ChatGPT: get the full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site.

Get a free API key

CMI Cosmetic Manufacturers Inc. FDA Warning Letters

1 warning letter on Apr 25, 2013.

IssuedSubjectIssuing officeClose-out letter
Apr 25, 2013 · Record page

A warning letter is FDA's formal notice that a company has violated FDA requirements. Each date links to the letter on fda.gov where FDA has it online. Search the text of every letter with the FDA warning letter search.

Recent FDA inspections

1 inspection on Oct 24, 2012.

DateSiteProductClassificationFEI
Oct 24, 2012Concord, CanadaDrugsOfficial Action Indicated (OAI)3003420009
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.

Compliance Actions

FDA's compliance actions data lists 1 compliance action under CMI Cosmetic Manufacturers Inc.: warning letters, injunctions and seizures. None came from FDA's Center for Tobacco Products.

Most recent: Warning Letter, Apr 25, 2013.

The warning letters in this data are listed above, together with the letters FDA posts online; a letter found in both is shown once. Other actions are not listed on this page. Search them with the FDA warning letter search or browse all compliance actions.

FDA-inspected facilities

1 inspected site, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3003420009Concord, Canada1Oct 24, 2012

CMI Cosmetic Manufacturers Inc. and the FDA: common questions

Has CMI Cosmetic Manufacturers Inc. received an FDA warning letter?

Yes. FDA has issued 1 warning letter to CMI Cosmetic Manufacturers Inc.. The most recent is dated Apr 25, 2013.

Has CMI Cosmetic Manufacturers Inc. received an FDA Form 483?

FDA has not published a Form 483 for "CMI Cosmetic Manufacturers Inc." in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect CMI Cosmetic Manufacturers Inc.?

The most recent FDA inspection on file ended Oct 24, 2012 at Concord, Canada and was classified OAI. FDA has 1 inspection of CMI Cosmetic Manufacturers Inc. on file, 1 of them classified OAI (official action indicated).

Need more than this page shows? Ask about CMI Cosmetic Manufacturers Inc. in Claude or ChatGPT and get every site's inspections, Form 483s, warning letters and import alerts, with a link to the FDA source for each record. The API key is free: no card.

Get a free API key

Prefer a PDF? Request a free supplier snapshot.

Is this your company or a supplier you list? Link to this FDA record from your site with a free button.

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