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