Form 3500-2025

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The document is a California Form 3500 Exemption Application, which organizations must complete to apply for tax-exempt status in California. It includes sections for organizational information, representative details, and specific questions regarding the organization's structure, activities, financial data, and compliance with state regulations. The form requires detailed descriptions of the organization's purpose, past and planned activities, financial statements, and information about officers and directors. Additionally, it outlines requirements for various types of organizations seeking exemption under different sections of the California Revenue and Taxation Code.

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Versions	Form popularity	Fillable & printable
2023	4.1 Satisfied (39 Votes)
2021	4.1 Satisfied (59 Votes)
2020	4.8 Satisfied (101 Votes)
2019	4.2 Satisfied (48 Votes)
2018	4.4 Satisfied (335 Votes)
2016	4.4 Satisfied (685 Votes)
2015	4 Satisfied (36 Votes)
2014	4 Satisfied (28 Votes)
2013	4 Satisfied (35 Votes)
2011	4 Satisfied (37 Votes)

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What is the purpose of the FDA form?

The Form FDA 483 notifies the companys management of observed objectionable conditions. At the conclusion of an inspection, the Form FDA 483 is presented and discussed with the companys senior management.

How much is the fee for form 3500 in California?

Application Fees: The $25 application fee is no longer required for FTB 3500 filed on or after 01/01/2021. Filing Fees: The $10 filing fee and the $25 late return filing fee are no longer required for Form 199 due on or after 01/01/2021, regardless of when the returns are actually filed.

What is a form 3500?

The purpose of form FTB 3500 is to apply for tax-exempt status from California franchise and income tax. If the organization provides all answers and documents required, the FTB will determine if the organization qualifies for tax‑exempt status.

How many days must a FDA mandatory reporting form 3500A be submitted to the FDA?

Initial reporting: Any unanticipated adverse event suspected to be caused/associated with a device must be reported to the FDA and the reviewing IRB within 10 working days of the event.

What is the FDA form 3500 used for?

Form FDA 3500 may be used by health professionals or consumers for VOLUNTARY reporting of adverse events, product use/medication errors, product quality problems, and therapeutic failures for: Prescription and over-the-counter medicines including those administered in a hospital or outpatient infusion centers.

What is FS form 3500?

The FS Form 3500 is used by individuals or organizations to provide a detailed list of securities. It is a continuation sheet and should be used in conjunction with the FS Form. The document requires information such as issue date, face amount and bond number.

Form 3500-2025

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