MedisourceRx
Letter data
- Company
- MedisourceRx
- Recipient
- Daniel D. Hernandez | Director of Quality | MedisourceRx | 10525 Humbolt Street | Los Alamitos | , | CA | 90720-5401 | United States
- Issue date
- 2026-07-27
- Posted date
- Not available
- FDA office
- Center for Drug Evaluation and Research (CDER)
- Subject
- Not available
- Product
- Drugs
- CMS ID
- 717970
- 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
MedisourceRx
MARCS-CMS 717970 —
July 27, 2026
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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
Content current as of:
07/30/2026
Regulated Product(s)
Drugs