FDA Letter API

Signature Biologics, LLC

Letter data

Company
Signature Biologics, LLC
Recipient
Neil H. Riordan, Ph.D. | Chief Executive Officer | Signature Biologics, LLC | 4040 W. Royal Lane, Suite 100 | Irving | , | TX | 75063-2844 | United States | neil@aidanresearch.com
Issue date
2025-02-21
Posted date
Not available
FDA office
Division of Biological Products Operations II
Subject
Not available
Product
Biologics
CMS ID
631039
Reference number
Not available
FEI
Not available
Inspection dates
Not available

Normalized citations

21 CFR: None found

21 U.S.C.: None found

Related FDA links

No related FDA letter link is present in the source index.

Full source text

CLOSEOUT LETTER Signature Biologics, LLC MARCS-CMS 631039 — February 21, 2025 More Warning Letters Warning Letters About Warning and Close-Out Letters Delivery Method: Via Email Product: Biologics Recipient: Recipient Name Neil H. Riordan, Ph.D. Recipient Title Chief Executive Officer Signature Biologics, LLC 4040 W. Royal Lane, Suite 100 Irving , TX 75063-2844 United States neil@aidanresearch.com Issuing Office: Division of Biological Products Operations II United States Secondary Issuing Offices United States Dear Dr. Neil H. Riordan: The United States Food and Drug Administration (FDA) has reviewed your firm’s corrective actions in response to Warning Letter #OBPO 23-631039 issued to you on September 18, 2023. Based on our evaluation of your response, your cessation of manufacture and distribution of Signature Matrix, Signature MatrixHX, and Signature Cord, and your destruction of product inventory, it appears that you have addressed the violation(s) detailed in the Warning Letter. Future FDA inspections and regulatory activities will further assess the adequacy and sustainability of your corrective actions. This letter does not relieve you or your firm from the responsibility of taking all necessary steps to ensure sustained compliance with the Federal Food, Drug, and Cosmetic Act, the Public Health Service Act, their implementing regulations, or other relevant legal authority. The Agency expects you and your firm to maintain compliance and will continue to monitor your state of compliance. This letter will not preclude any future regulatory action should violations be observed during a subsequent inspection or through other means. Sincerely, /S/ Melissa J. Mendoza Director Office of Compliance and Biologics Quality Center for Biologics Evaluation and Research Content current as of: 03/06/2025 Regulated Product(s) Biologics