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Selder S.A. de C.V.

Selder S.A. de C.V.

United States

Issuing Office:

United States


Department of Health and Human Services' logoDepartment of Health and Human Services

Public Health Service
Food and Drug Administration
 Office of Manufacturing and Product Quality
Division of International Drug Quality
10903 New Hampshire Avenue
Building #51, Room 4223
Silver Spring, MD 20993

TELEPHONE: (240) 402-4179
                 FAX: (301) 847-8742


March 28, 2014

Mr. Alejandro Martinez Villarreal
Director General
Selder S.A de C.V.
Fernando Villalpando #48
Colonia Guadalupe Inn
Mexico DF, Mexico 01020

References: FEI 3001362772

Dear Mr. Villarreal:

The Food and Drug Administration has completed the evaluation of your firm’s corrective actions in response to our Warning Letter WL # 320-12-17 dated April 27, 2012. Based on our evaluation, it appears that you have addressed the violations contained in this Warning Letter. Future FDA inspections and regulatory activities will further assess the adequacy and sustainability of these corrections.

This letter does not relieve you or your firm from the responsibility of taking all necessary steps to assure sustained compliance with the Federal Food, Drug, and Cosmetic Act and its implementing regulations or with other relevant legal authority. The Agency expects you and your firm to maintain compliance and will continue to monitor your state of compliance. This letter will not preclude any future regulatory action should violations be observed during a subsequent inspection or through other means.




/Xiaohui Shen/
Compliance Officer
Division of International Drug Quality

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