Medtronic, Inc.

Warning LetterOpen

United StatesFEI 3015180993Issued Dec 9, 2021Center for Devices and Radiological Health

View Letter

Source: FDA, published letter. FDA published this warning letter; View Letter opens FDA's copy. To check it, open FDA's record for this establishment, listed under FEI 3015180993.

Violations0

Issue DateDec 9, 2021

Product TypeMedical Devices

StatusOpen

Letter Details

Firm: Medtronic, Inc.
Location: United States
FEI Number: 3015180993
Country: United States
Issue Date: December 09, 2021
Issuing Office: Center for Devices and Radiological Health
Product Type: Medical Devices
Status: Open

Summary

Based on limited metadata, Medtronic, Inc., a medical device manufacturer, received an FDA Warning Letter on December 9, 2021. Without access to the full letter text or specific subject line, the exact nature of the violations cannot be determined from the available information. The warning pertains to medical devices regulated by the FDA, though the specific issuing office and violation details are not available in this metadata summary.

Medtronic, Inc. FDA Warning Letter, December 9, 2021