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Were n d moditied to adversely affed perfomwar and we m n h e d In accwdana pmvia ls d21 CFFi Patl 1020 1ao affirm that. COMPONENT INFORMATION If additional space. is needsd for this section use enother form replacing the preprinted number with this Form Number andcomplete I t e m 1 4 and 5 on a T H E W E R CONTROLIS R CONTROLMANUFACTURER a DATE MANUFACTURED d. A PRINTED NAME DATE -FORM FDA 2579 I m l o w o r n c mtsosw m d --- bibw Copy - State Age f P. -w m.is-. STREET ADDRESS C. crry D...
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FDA use only refers to information or documentation that is intended for internal use by the FDA and should not be disclosed to the public or other external parties.
Companies or individuals that are submitting documents or information to the FDA may be required to indicate certain parts of their submission as for FDA use only.
To fill out for FDA use only, simply mark the relevant sections or documents with a clear indication that they are intended for FDA use only.
The purpose of marking information as for FDA use only is to ensure that sensitive or confidential information is protected and only accessible to authorized FDA personnel.
Information that is proprietary, confidential, or otherwise sensitive in nature should be reported on for FDA use only to protect it from public disclosure.
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