FDA Letter API

Abraxis Bioscience LLC

Letter data

Company
Abraxis Bioscience LLC
Recipient
Nathan Trembath | General Manager | Abraxis Bioscience LLC | 620 N 51 St. Ave. | Phoenix | , | AZ | 85043 | United States
Issue date
2024-01-18
Posted date
Not available
FDA office
Center for Drug Evaluation and Research | CDER
Subject
Not available
Product
Drugs
CMS ID
633713
Reference number
Not available
FEI
3006441852
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 Abraxis Bioscience LLC MARCS-CMS 633713 — January 18, 2024 More Warning Letters Warning Letters About Warning and Close-Out Letters Reference #: FEI 3006441852 Product: Drugs Recipient: Recipient Name Nathan Trembath Recipient Title General Manager Abraxis Bioscience LLC 620 N 51 St. Ave. Phoenix , AZ 85043 United States Issuing Office: Center for Drug Evaluation and Research | CDER United States Secondary Issuing Offices United States Dear Mr. Trembath: The Food and Drug Administration (FDA) has completed an evaluation of your firm’s corrective actions in response to our Warning Letter # 633713 dated October 31, 2022. Based on our evaluation, it appears that you have addressed the violation 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/ Joan Johnson Compliance Officer Division of Drug Quality I Content current as of: 03/25/2024 Regulated Product(s) Drugs