by ComplianceQuest

Inspection Tracker

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

FDA Guidance Global Templates

Start with a Free ConsultationBook 30 minutes with a ComplianceQuest specialist.Book a Call

Sign In Create a Free Account

Big News: FDA is moving from MasterControl to ComplianceQuest.See Why

Search AgentQ/

Talk to a Specialist

Loading…

My DashboardInspection TrackerWarning LettersPeter Schiff Enterprises

All Warning Letters

Peter Schiff Enterprises

Warning LetterOpen

4400 Log Cabin Ln. Cookeville , TN 38506 United States, (b)(6), (b)(7)(C)Issued Aug 26, 2026Center for Devices and Radiological Health

Source: FDA, published letter. FDA published this warning letter; View Letter opens FDA's copy.

Violations18

Issue DateAug 26, 2026

Product TypeMedical Devices

StatusOpen

Letter Details

Firm: Peter Schiff Enterprises
Location: 4400 Log Cabin Ln. Cookeville , TN 38506 United States, (b)(6), (b)(7)(C)
FEI Number: N/A
Country: United States
Issue Date: August 26, 2026
Issuing Office: Center for Devices and Radiological Health
Product Type: Medical Devices
Status: Open

Subject

Medical Device/Adulterated/Misbranded/Lacks PMA and/or 510(k)

Peter Schiff Enterprises FDA Warning Letter, August 26, 2026