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Hofmann X-Ray of America, Inc.

FDA Regulatory Profile

Hofmann X-Ray of America, Inc. appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 20, 1989.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K893690SUPER SPEED POTTER-BUCKY (ESO5-110 & 220)July 20, 1989
K851011HOFMANN G-S60 SINGLE PHASE X-RAY GENERATORApril 10, 1985

FDA data resources