Synovo Production, Inc.

Warning LetterOpen

United StatesFEI 2280596Issued Mar 23, 2023Division of Medical Device and Radiological Health Operations West

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 2280596.

Violations0

Issue DateMar 23, 2023

Product TypeMedical Devices

StatusOpen

Letter Details

Firm: Synovo Production, Inc.
Location: United States
FEI Number: 2280596
Country: United States
Issue Date: March 23, 2023
Issuing Office: Division of Medical Device and Radiological Health Operations West
Product Type: Medical Devices
Status: Open

Summary

Based on limited metadata, Synovo Production, Inc. received an FDA Warning Letter on March 23, 2023, regarding medical devices. Without access to the full warning letter text or specific subject line details, the exact nature of the violations cannot be determined from the available information. The letter was issued by the FDA's medical devices regulatory authority, though the specific issuing office is not identified in this metadata summary.

Synovo Production, Inc. FDA Warning Letter, March 23, 2023