Supplier due-diligence record
FDA Supplier Evidence Snapshot
Turn a live Import Alert Radar result into a dated, source-linked record you can retain with your supplier review.
Selected FDA firm
GFA Production Xiamen Co., Ltd.
China
3
Red-list alerts
0
Green-list alerts
0
Yellow-list alerts
2026-09-04
Dataset checked
Live preview of matched records
- REDIA 55-0502/16/2023
Detention Without Physical Examination Of Finished Dosage Form Drug Products, Active Pharmaceutical Ingredients, and Inactive Ingredients for Potentially Hazardous Microbiological Contamination
Official FDA record ↗ - REDIA 66-4006/12/2024
Detention Without Physical Examination of Drugs From Firms Which Have Not Met Drug GMPs
Official FDA record ↗ - REDIA 89-0811/07/2024
Detention Without Physical Examination of Devices without Approved PMA's or IDE's and Other Devices Not Substantially Equivalent or Without a 510(k)
Official FDA record ↗
Your delivered record includes
- Exact firm name and country used for the FDA match.
- Current Red / Green / Yellow List finding and every matched import alert.
- Firm-entry dates, official FDA source links and dataset timestamp.
- Human review of the firm match and a printable PDF delivered by email.