Dairies and places of meat inspection regulated by the Department of Food and Agriculture. See Section 1.6 for additional scope provisions. 6. ...
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1.1.3.2 State-regulated buildings, structures, and applications
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1.1.3.2 State-regulated buildings, structures, and applications
Dairies and places of meat inspection regulated by the Department of Food and Agriculture. See Section 1.6 for additional scope provisions. ...
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PEDESTRIAN
[DSA-AC] An individual who moves in walking areas with or without the use of walking assistive devices such as crutches, leg braces, wheelchairs, white cane, service animal, etc....
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Usable
Usable: For a product or service to be usable, people with disabilities must be able to learn about and operate the product's or service's features effectively....
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Background
is the responsibility of the architects, engineers, interior designers, landscape architects, contractors, subcontractors, vendors, product manufacturers, building owners and managers, service...
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10. Prescription Drug Container Labels
This initiative was authorized by the “Food and Drug Administration Safety and Innovation Act" which President Obama signed into law in July 2012. ...
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10. Prescription Drug Container Labels
This initiative was authorized by the “Food and Drug Administration Safety and Innovation Act" which President Obama signed into law in July 2012. ...
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10. Prescription Drug Container Labels
This initiative was authorized by the “Food and Drug Administration Safety and Innovation Act" which President Obama signed into law in July 2012. ...
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Stories of Emergency Use of Mobile Devices
“We’ve also heard from parents of children with food allergies, thanking us for creating the app that saved their child’s life.”...
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1011.2.1 Size and Location
The usable sides of these elements are the sides that can be used for eating or serving food, building a fire, or cooking....
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10. Prescription Drug Container Labels
This initiative was authorized by the “Food and Drug Administration Safety and Innovation Act" which President Obama signed into law in July 2012. ...
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3.1 Refining MDE Definition and Committee Scope
They started with the definition of “medical device” used by the Food and Drug Administration (FDA, Box 3.1)....
- inLOOP Commercial Use Loop Listener #01115