Mylan Laboratories Limited Unit 8, a Viatris Company

CLOSEOUT LETTER Mylan Laboratories Limited Unit 8, a Viatris Company MARCS-CMS 589297 — July 27, 2023 More Warning Letters Warning Letters About Warning and Close-Out Letters Reference #: FEI 3002785310 Product: Drugs Recipient: Recipient Name Mr. Scott A. Smith Recipient Title Chief Executive Officer Mylan Laboratories Limited Unit 8, a Viatris Company Viatris Inc. 1000 Mylan Boulevard Canonsburg , PA 15317 United States Issuing Office: Center for Drug Evaluation and Research | CDER United States Dear Mr. Smith: The Food and Drug Administration (FDA) has completed an evaluation of your firm’s corrective actions in response to our Warning Letter 320-20-06 dated November 5, 2019. Based on our evaluation, it appears that you have addressed the deviations 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 firm 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 FDA expects you and your firm to maintain compliance and will continue to monitor your state of compliance. This letter will not preclude any future regulatory action should deviations be observed during a subsequent inspection or through other means. Sincerely, /S/ Tamara Rosbury, Ph.D. Compliance Officer Division of Drug Quality II Content current as of: 08/01/2023 Regulated Product(s) Drugs