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Medcraft Corp.

FDA Regulatory Profile

Medcraft Corp. has 0 FDA recalls, 1 inspection, 5 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jul 27, 2018 · VAI
Latest 510(k)
Nov 10, 1986

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances5Oct 4, 2026Not statedCurrent
Inspections1Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 27, 2018Mounds, OKDrugsVoluntary Action Indicated (VAI)3013329127

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.

Recent 510(k) Clearances

K-NumberDeviceDate
K860467ELECTROSHOCK UNIT NEUROLOGY MODEL B-25Nov 10, 1986
K791795COMP-ACT IVSep 27, 1979
K760508ACCUTAPE 24Aug 30, 1976
K760509TREADMILL, DIAGNOSTICAug 30, 1976
K760510MONITORING SYSTEM, REHABILITATIONAug 30, 1976

FDA data resources