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Notice

Foreign-Trade Zone (FTZ) 35, Notification of Proposed Production Activity; PCI Pharma Services; (Pharmaceutical Products); Croydon and Philadelphia, Pennsylvania

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Key Dates
Citation: 89 FR 94704
Public Participation

In Plain English

What is this Federal Register notice?

This is a notice published in the Federal Register by Commerce Department, Foreign-Trade Zones Board. Notices communicate information, guidance, or policy interpretations but may not create new binding obligations.

Is this rule final?

This document is classified as a notice. It may or may not create enforceable regulatory obligations depending on its specific content.

Who does this apply to?

Consult the full text of this document for specific applicability provisions. The affected parties depend on the regulatory scope defined within.

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Why it matters: This notice communicates agency policy or guidance regarding applicable regulations.

Document Details

Document Number2024-28024
FR Citation89 FR 94704
TypeNotice
PublishedNov 29, 2024
Effective Date-
RIN-
Docket IDB-58-2024
Pages94704–94704 (1 pages)
Text FetchedYes

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Related Documents (by RIN/Docket)

Doc #TypeTitlePublished
2025-05115 Notice Foreign-Trade Zone (FTZ) 35; Authorizati... Mar 26, 2025

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Full Document Text (237 words · ~2 min read)

Text Preserved
<NOTICE> DEPARTMENT OF COMMERCE <SUBAGY>Foreign-Trade Zones Board</SUBAGY> <DEPDOC>[B-58-2024]</DEPDOC> <SUBJECT>Foreign-Trade Zone (FTZ) 35, Notification of Proposed Production Activity; PCI Pharma Services; (Pharmaceutical Products); Croydon and Philadelphia, Pennsylvania</SUBJECT> PCI Pharma Services (PCI) submitted a notification of proposed production activity to the FTZ Board (the Board) for its facilities in Croydon, Pennsylvania and Philadelphia, Pennsylvania within Subzone 35L. The notification conforming to the requirements of the Board's regulations (15 CFR 400.22) was received on November 21, 2024. Pursuant to 15 CFR 400.14(b), FTZ production activity would be limited to the specific foreign-status material(s)/component(s) and specific finished product(s) described in the submitted notification (summarized below) and subsequently authorized by the Board. The benefits that may stem from conducting production activity under FTZ procedures are explained in the background section of the Board's website—accessible via <E T="03">www.trade.gov/ftz.</E> The proposed finished product includes: cendakimab dosages packed in single and multi-dose packaging (duty-free). The proposed foreign-status material/component includes: bulk cendakimab in filled syringes (duty-free). Public comment is invited from interested parties. Submissions shall be addressed to the Board's Executive Secretary and sent to: <E T="03">ftz@trade.gov.</E> The closing period for their receipt is January 8, 2025. A copy of the notification will be available for public inspection in the “Online FTZ Information System” section of the Board's website. For further information, contact Kolade Osho at <E T="03">Kolade.Osho@trade.gov.</E> <SIG> <DATED>Dated: November 22, 2024.</DATED> <NAME>Elizabeth Whiteman,</NAME> Executive Secretary. </SIG> <FRDOC>[FR Doc. 2024-28024 Filed 11-27-24; 8:45 am]</FRDOC> </NOTICE>
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