Atlas FDA

Trexo Robotics Holdings Inc.

FDA warning letter issued 2024-02-07 · posted 2024-06-04

Letter details

Company
Trexo Robotics Holdings Inc.
Subject
Investigational Device Exemptions (IDE)/Premarket Approval Application (PMA) Adulterated Device, Misbranded
Issuing office
OHT5: Office of Neurological and Physical Medicine Devices, Office of Product Evaluation and Quality
Letter issue date
2024-02-07
Posted date
2024-06-04
Case number
673150

Read the full letter on fda.gov

FDA's public listing keeps roughly five years of letters; older ones roll off. Atlas preserves every letter it has ingested since September 2026 and refreshes the listing weekly. Verify enforcement matters against the primary source linked above.

Hear about the next one

Watch an issuing office from its directory page and new letters land in your change alerts. Elsewhere this data sells for hundreds of dollars per document; here it is part of the record.