Import Refusal Report
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Refusal Details as Recorded in OASIS by FDA
for Refusal 275-1421292-0/13/1
| Manufacturer FEI | 2024312 | ||||||
|---|---|---|---|---|---|---|---|
| Manufacturer Name | Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical | ||||||
| Manufacturer Address line 1 | 1717 W Collins Ave | ||||||
| Manufacturer Address line 2 | |||||||
| Manufacturer's City | Orange | ||||||
| Manufacturer Province/State | CA | ||||||
| Manufacturer Country/Area | United States | ||||||
| Product Code | 76EKM | ||||||
| Importer's Product Description | REAL SEAL CARTRIDGE (GUTTA PERCHA) RETURN FOR CREDIT AND RESTOCK | ||||||
| Refusal Date | 23-Sep-2010 | ||||||
| FDA District | LOS-DO | ||||||
| Entry/doc/line/sfx | 275-1421292-0/13/1 | ||||||
| FDA Sample Analysis | No | ||||||
| FDA Record of Private Lab Sample Analysis | No | ||||||
| Charge(s) |
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