FDA Import Refusal AEK-5875622-0/11/1 — HOMEOLIFE CLINIC
The FDA refused shipment AEK-5875622-0/11/1 from HOMEOLIFE CLINIC (India) on Nov 1, 2024. The refused product falls under Drugs and Biologics — ALBUMIN IODINATED I-125 SERUM. Cited charge: 75 This firm has 5 or more other import refusals on record.
Refusal details
- Date
- Nov 1, 2024
- Country
- India
- Product Category
- Drugs and Biologics
- Product Code
- 58GDY02 ALBUMIN IODINATED I-125 SERUM
- Charges
- 75