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Get the free 483 3 SERIES OF 2009 COMMITTEE OF REFERENCE: Neighborhood Community &amp - denve...

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This document is an ordinance approving an agreement between the City and County of Denver and Neighborhood Development Collaborative, Inc. for implementing program activities related to the Neighborhood
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483 3 series refers to Form FDA 483, which is used by the Food and Drug Administration (FDA) to document observations made during inspections of regulated facilities.
Regulated facilities, such as pharmaceutical manufacturers, food processors, and medical device manufacturers, are required to file Form FDA 483.
When filling out Form FDA 483, the inspector documents any observations of non-compliance with FDA regulations and includes specific details about the observed deficiencies.
The purpose of Form FDA 483 is to provide a written record of observations made during an inspection, serve as a basis for further regulatory action, and encourage voluntary compliance with FDA regulations.
The Form FDA 483 must report observations or deviations from applicable regulations, including details such as the date, location, and description of the observed deficiencies.
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