Greiner Bio-One North America, Inc.

Warning LetterOpen

United StatesFEI 3001451379Issued Apr 16, 2020

View FDA's record for FEI 3001451379

Source: FDA warning letter records. FDA has not published the text of this letter. To check it, open FDA's record for this establishment, listed under FEI 3001451379.

Violations0

Issue DateApr 16, 2020

Product TypeMedical Devices

StatusOpen

Letter Details

Firm: Greiner Bio-One North America, Inc.
Location: United States
FEI Number: 3001451379
Country: United States
Issue Date: April 16, 2020
Issuing Office: N/A
Product Type: Medical Devices
Status: Open

Summary

Based on limited metadata, this FDA Warning Letter issued to Greiner Bio-One North America, Inc. on April 16, 2020, concerns medical devices manufactured by the company. Without access to the full letter text or subject line, the specific nature of the violations cannot be determined from the available information. The warning falls under FDA's medical device regulatory authority, though the specific issuing office is not identified in the metadata provided.

Greiner Bio-One North America, Inc. FDA Warning Letter, April 16, 2020