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  5. Leisegang Feinmechanick-Optik GmbH - 05/26/2016
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Leisegang Feinmechanick-Optik GmbH

Leisegang Feinmechanick-Optik GmbH

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
 10903 New Hampshire Avenue
Silver Spring, MD 20993

Via United Parcel Service

MAY 26, 2016

Uwe Skirl
Manager Director
Leisegang Feinmechanik-Optk GmbH
Leibnizstrasse 32
Berlin 10625

Dear Mr. Skirl:

The Food and Drug Administration (FDA) has completed an evaluation of your firm's corrective actions in response to our Warning Letter #305239. 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.

Carl Fischer, Ph.D.
Division of International Compliance
Office of Compliance
Center for Devices and Radiological Health

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