company
Inter-Med Llc
Jurisdiction: US
FDA Warning Letter timeline
V1 scope: FDA Warning Letters only. Additional public-record sources (SEC, CPSC, federal contracts) are on the V2 roadmap and are not surfaced here today.
- fda_recall · device_recall2026-06-17Inter-Med Llc — Class II recall: Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-2…
Frequently asked questions
- How many FDA warning letters has Inter-Med Llc received?
- Argus HQ has not recorded an FDA warning letter for Inter-Med Llc in our current dataset.
- What FDA recalls has Inter-Med Llc issued?
- Argus HQ has recorded 1 FDA recall tied to Inter-Med Llc.
- Is Inter-Med Llc FDA compliant?
- Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 1 recall, and 0 approval records for Inter-Med Llc. Review the linked FDA source records directly before drawing a compliance conclusion.
Informational only. FDA Warning Letters are public records (17 USC §105). Summaries are AI-assisted and may contain errors; always verify against the original FDA letter before acting. Not legal, financial, or regulatory advice.

