FDA Letter API

Davati Medical Supply LLC

Letter data

Company
Davati Medical Supply LLC
Recipient
Philip Quick | Vice President of Operations | Davati Medical Supply LLC | 3121 Eagles Nest St. | Suite 120 | Round Rock | , | TX | 78665 | United States | pquick@davatimedical.com
Issue date
2021-10-14
Posted date
Not available
FDA office
Center for Biologics Evaluation and Research (CBER)
Subject
Not available
Product
Biologics
CMS ID
615530
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 Davati Medical Supply LLC MARCS-CMS 615530 — October 14, 2021 More Warning Letters Warning Letters About Warning and Close-Out Letters Delivery Method: Via Express Delivery and Electronic Mail Product: Biologics Recipient: Recipient Name Philip Quick Recipient Title Vice President of Operations Davati Medical Supply LLC 3121 Eagles Nest St. Suite 120 Round Rock , TX 78665 United States pquick@davatimedical.com Issuing Office: Center for Biologics Evaluation and Research (CBER) United States Dear Mr. Quick: The United States Food and Drug Administration (FDA) has completed evaluation of your firm’s corrective actions in response to the Warning Letter (#CBER 21-02) issued by FDA to Davati Medical Supply, LLC on June 26, 2021. Based on our evaluation, it appears that you have addressed the violation(s) contained in this WL. 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 Agency 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 violations be observed during a subsequent inspection or through other means. If you have any questions regarding this letter, please contact the Division of Case Management, CBER at (240) 402-9155 or CBERDCMRecommendations@fda.hhs.gov. Please be advised that only written communications are considered official. Sincerely, /S/ Mary A. Malarkey Director Office of Compliance and Biologics Quality Center for Biologics Evaluation and Research Office of Compliance and Biologics Quality Content current as of: 10/14/2021 Regulated Product(s) Biologics