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Jpi America, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K052341
AJEX 9015/135H PORTABLE X-RAY
October 7, 2005
K945328
JPI X-RAY FILM CASSETTE
January 20, 1995
K945327
JPI X-RAY GRID
January 20, 1995