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Phamedica, Inc.

FDA Regulatory Profile

Phamedica, Inc. has 0 FDA recalls, 2 inspections, 1 510(k) clearance and 0 compliance actions on record.

Latest inspection
Dec 10, 2021 · NAI
Latest 510(k)
Jun 29, 2017

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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) clearances1Oct 4, 2026Not statedCurrent
Inspections2Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Dec 10, 2021Plainview, NYDevicesNo Action Indicated (NAI)3011848308
Jan 10, 2020Plainview, NYDevicesVoluntary Action Indicated (VAI)3011848308

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
K163011PHA S1 Spinal SystemJun 29, 2017

FDA data resources