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