FDA Letter API

Furst-McNess Company

Letter data

Company
Furst-McNess Company
Recipient
Mark Poeschl | CEO | Furst-McNess Company | 1252 Bell Valley Road, Suite 220 | Rockford | , | IL | 61108 | United States | jeff.davidson@mcness.com
Issue date
2026-04-30
Posted date
Not available
FDA office
Division of Human and Animal Food Operations West I
Subject
Not available
Product
Animal & Veterinary
CMS ID
668925
Reference number
Not available
FEI
Not available
Inspection dates
Not available

Normalized citations

21 CFR: None found

21 U.S.C.: None found

Related FDA links

No related FDA letter link is present in the source index.

Full source text

CLOSEOUT LETTER Furst-McNess Company MARCS-CMS 668925 — April 30, 2026 More Warning Letters Warning Letters About Warning and Close-Out Letters Delivery Method: VIA EMAIL NO HARD COPY TO FOLLOW Product: Animal & Veterinary Recipient: Recipient Name Mark Poeschl Recipient Title CEO Furst-McNess Company 1252 Bell Valley Road, Suite 220 Rockford , IL 61108 United States jeff.davidson@mcness.com Issuing Office: Division of Human and Animal Food Operations West I United States Secondary Issuing Offices United States Dear Mark Poeschl, The United States Food and Drug Administration has completed evaluation of your facility’s corrective actions in response to our Warning Letter CMS 668925, dated March 12, 2024. Based on our evaluation, it appears that you have addressed the violations contained in this Warning Letter. Future FDA inspections and regulatory activities will further assess the adequacy and sustainability of these corrections. This letter does not relieve you or your facility from the responsibility of taking all necessary steps to assure sustained compliance with the Federal Food, Drug, and Cosmetic Act and its implementing regulations or with other relevant legal authority. The Agency expects you and your facility to maintain compliance and will continue to monitor your state of compliance. This letter will not preclude any future regulatory action should violations be observed during a subsequent inspection or through other means. Sincerely, /S/ CDR Kelli Wilkinson Branch Director, Office of Surveillance and Compliance Center for Veterinary Medicine U.S. Food and Drug Administration Content current as of: 05/04/2026 Regulated Product(s) Animal & Veterinary