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VIANT COSTA RICA, S.A. FDA Record

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

VIANT COSTA RICA, S.A. has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 1 compliance action on record. FDA has issued 1 warning letter to VIANT COSTA RICA, S.A., the most recent on Jul 1, 2014.

What these totals cover: FDA records filed under the name "VIANT COSTA RICA, S.A." and its spelling variant "Viant Costa Rica".

Latest inspection: Aug 6, 2015 · NAI

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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	4	Nov 14, 2026	Newest record Nov 5, 2026	Current
Compliance actions	1	Nov 2, 2026	Newest record Oct 29, 2026	Current

VIANT COSTA RICA, S.A. FDA Warning Letters

1 warning letter on Jul 1, 2014.

Issued	Subject	Issuing office	Close-out letter
Jul 1, 2014

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

4 inspections from Jul 2, 2009 to Aug 6, 2015.

Date	Site	Product	Classification	FEI
Aug 6, 2015	Barreal De Heredia, Costa Rica	Devices	No Action Indicated (NAI)	3005173255
Mar 6, 2014	Barreal De Heredia, Costa Rica	Devices	Official Action Indicated (OAI)	3005173255
Aug 9, 2011	Barreal De Heredia, Costa Rica	Devices	No Action Indicated (NAI)	3005173255
Jul 2, 2009	Barreal De Heredia, Costa Rica	Devices	No Action Indicated (NAI)	3005173255

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 VIANT COSTA RICA, S.A.: warning letters, injunctions and seizures. None came from FDA's Center for Tobacco Products.

Most recent: Warning Letter, Jul 1, 2014.

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 3005173255	Barreal De Heredia, Costa Rica	4	Aug 6, 2015

VIANT COSTA RICA, S.A. and the FDA: common questions

Has VIANT COSTA RICA, S.A. received an FDA warning letter?

Yes. FDA has issued 1 warning letter to VIANT COSTA RICA, S.A.. The most recent is dated Jul 1, 2014.

Has VIANT COSTA RICA, S.A. received an FDA Form 483?

FDA has not published a Form 483 for "VIANT COSTA RICA, S.A." in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect VIANT COSTA RICA, S.A.?

The most recent FDA inspection on file ended Aug 6, 2015 at Barreal De Heredia, Costa Rica and was classified NAI. FDA has 4 inspections of VIANT COSTA RICA, S.A. on file, 1 of them classified OAI (official action indicated).

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