Always More Marketing, Inc.

FDA Regulatory Profile

Always More Marketing, Inc. has 0 FDA recalls, 5 inspections, 4 510(k) clearances and 0 compliance actions on record.

Latest inspection
Oct 17, 2024 · NAI
Latest 510(k)
Jan 24, 2019

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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) clearances4Oct 4, 2026Not statedCurrent
Inspections5Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Oct 17, 2024Calabasas, CADevicesNo Action Indicated (NAI)3009549313
Sep 29, 2021Calabasas, CADevicesNo Action Indicated (NAI)3009549313
Aug 10, 2018Calabasas, CADevicesVoluntary Action Indicated (VAI)3009549313
Nov 15, 2016Calabasas, CADevicesNo Action Indicated (NAI)3009549313
Sep 12, 2013Calabasas, CADevicesVoluntary Action Indicated (VAI)3009549313

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
K182312Zyppah Anti-Snoring DeviceJan 24, 2019
K120372DR GREENBURGS HYBRID VACUUMJun 27, 2012
K120371DR GREENBURGS HYBRID ACRYLICJun 27, 2012
K111680DR. GREENSBURG'S HYBRIDDec 23, 2011