FDA Letter API

B. Braun Medical Inc.

Letter data

Company
B. Braun Medical Inc.
Recipient
Peter A. Klaes | Vice President and General Manager, Irvine Operations | B. Braun Medical Inc. | 2525 McGaw Avenue | Irvine | , | CA | 92614-5841 | United States
Issue date
2020-10-22
Posted date
Not available
FDA office
Los Angeles District Office
Subject
Not available
Product
Not available
CMS ID
501232
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 B. Braun Medical Inc. MARCS-CMS 501232 — October 22, 2020 More Warning Letters Warning Letters About Warning and Close-Out Letters Delivery Method: VIA UPS Recipient: Recipient Name Peter A. Klaes Recipient Title Vice President and General Manager, Irvine Operations B. Braun Medical Inc. 2525 McGaw Avenue Irvine , CA 92614-5841 United States Issuing Office: Los Angeles District Office United States 949-608-2900 Dear Mr. Klaes: The U.S. Food and Drug Administration (FDA) has completed an evaluation of your firm’s corrective actions in response to our Warning Letter #30-17 dated May 12, 2017. 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 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 violations be observed during a subsequent inspection or through other means. Sincerely, /S/ CDR Steven E. Porter, Jr. Director, Division of Pharmaceutical Quality Operations IV Content current as of: 10/26/2020