1. Home
  2. Inspections, Compliance, Enforcement, and Criminal Investigations
  3. Compliance Actions and Activities
  4. Warning Letters
  5. MedisourceRx - 717970 - 07/27/2026
  1. Warning Letters

CLOSEOUT LETTER

MedisourceRx MARCS-CMS 717970 —

Delivery Method:
VIA ELECTRONIC MAIL READ/DELIVERY RECEIPT
Product:
Drugs

Recipient:
Recipient Name
Daniel D. Hernandez
Recipient Title
Director of Quality
MedisourceRx

10525 Humbolt Street
Los Alamitos, CA 90720-5401
United States

Issuing Office:
Center for Drug Evaluation and Research (CDER)

United States

Secondary Issuing Offices

United States


Dear Mr. Hernandez:

The U.S. Food and Drug Administration (FDA) has completed an evaluation of your firm’s corrective actions in response to our warning letter #717970, issued on December 12, 2025. Based on our evaluation, it appears that you have adequately addressed the violations contained in this warning letter.

You are expected to take all necessary steps to ensure compliance with the Federal Food, Drug, and Cosmetic Act and FDA’s implementing regulations. This letter will not preclude any future regulatory action should violations be observed during a subsequent inspection or through other means.


Sincerely,
/S/
Matthew J. Lash
Acting Director
Office of Compounding Quality and Compliance
Office of Compliance
Center for Drug Evaluation and Research

Back to Top