by ComplianceQuest

My Dashboard Inspection Tracker FDA Guidance Templates Assessments

Sign in Get started

Tracker Overview Enforcement Themes Form 483s Warning Letters Inspections Recalls Investigators Companies Facilities

ANALYTICS

Tracker Overview Enforcement Themes

FDA ACTIONS

Form 483s Warning Letters Inspections Recalls

AUDIT READINESS

COMPANIES

Companies Facilities

Loading…

Dashboard Warning LettersWarning Letter Details

ZIIP, Inc. Warning Letter Details

Warning Letter

ZIIP, Inc.

ZIIP, Inc., 2495 Estand Way Pleasant Hill , CA 94523-3911 United States, (b)(6), (b)(7)(C)

Issue DateMay 22, 2026

FEI NumberN/A

Violations10

CountryUnited States

Issuing Office

Center for Devices and Radiological Health

Product Type

Medical Devices

Status

Open

Subject

CGMP/QSR/Medical Devices/Adulterated

ZIIP, Inc. FDA Warning Letter, May 22, 2026