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MicroPort CRM S.R.L. FDA Record

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

MicroPort CRM S.R.L. has 0 FDA recalls, 3 inspections, 0 510(k) clearances and 1 compliance action on record. FDA has issued 1 warning letter to MicroPort CRM S.R.L., the most recent on Oct 29, 2009.

What these totals cover: FDA records filed under the name "MicroPort CRM S.R.L." and its spelling variant "Microport Crm".

Latest inspection: Mar 28, 2013 · VAI

Summary

Record counts and when each FDA source was last refreshed
Records	Count	Last refreshed	Source as of	Status
Recalls	0	Nov 8, 2026	File dated Nov 3, 2026	Current
510(k) clearances	0	Nov 8, 2026	File dated Nov 2, 2026	Current
Inspections	3	Nov 14, 2026	Newest record Nov 5, 2026	Current
Compliance actions	1	Nov 2, 2026	Newest record Oct 29, 2026	Current

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MicroPort CRM S.R.L. FDA Warning Letters

1 warning letter on Oct 29, 2009.

Issued	Subject	Issuing office	Close-out letter
Oct 29, 2009

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

3 inspections from Jul 2, 2009 to Mar 28, 2013.

Date	Site	Product	Classification	FEI
Mar 28, 2013	Saluggia, VC, Italy	Devices	Voluntary Action Indicated (VAI)	1000165971
Mar 3, 2011	Saluggia, VC, Italy	Devices	Voluntary Action Indicated (VAI)	1000165971
Jul 2, 2009	Saluggia, VC, Italy	Devices	Official Action Indicated (OAI)	1000165971

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 MicroPort CRM S.R.L.: warning letters, injunctions and seizures. None came from FDA's Center for Tobacco Products.

Most recent: Warning Letter, Oct 29, 2009.

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.

Facility	Location	Inspections	Latest
FEI 1000165971	Saluggia, VC, Italy	3	Mar 28, 2013

MicroPort CRM S.R.L. and the FDA: common questions

Has MicroPort CRM S.R.L. received an FDA warning letter?

Yes. FDA has issued 1 warning letter to MicroPort CRM S.R.L.. The most recent is dated Oct 29, 2009.

Has MicroPort CRM S.R.L. received an FDA Form 483?

FDA has not published a Form 483 for "MicroPort CRM S.R.L." in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect MicroPort CRM S.R.L.?

The most recent FDA inspection on file ended Mar 28, 2013 at Saluggia, VC, Italy and was classified VAI. FDA has 3 inspections of MicroPort CRM S.R.L. on file, 1 of them classified OAI (official action indicated).

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