Almore International Inc

FDA Regulatory Profile

Almore International Inc appears in FDA public data with 1 recall, 0 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent recall (Z-2069-2017, Class II) was initiated on April 20, 2017.

Summary

Total Recalls
1
510(k) Clearances
0
Inspections
1
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-2069-2017Class IIMicrofil Composite Instruments are packaged in an unsealed plastic sleeve, which is then placed in aApril 20, 2017