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FDA Inspection
•Baxter Pharmaceutical Solutions, LLC•September 23, 2010

Baxter Pharmaceutical Solutions, LLC – FDA Inspection, Sep 23, 2010

Record Details

This FDA Inspection record concerns Baxter Pharmaceutical Solutions, LLC, with an inspection on September 23, 2010, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Baxter Pharmaceutical Solutions, LLC
Inspection Date
September 23, 2010
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · f4da5ce7-e1e0-4a55-a3ab-fbc167114943

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
681949
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Baxter Pharmaceutical Solutions, LLC

19
DateClassificationOfficeProject area
December 11, 2025Not classifiedDetroit District OfficeBlood and Blood Products
September 24, 2024Not classifiedDetroit District Office
July 26, 2024Not classifiedDetroit District Office
February 20, 2024Not classifiedDetroit District Office
February 17, 2023NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 19 other inspections on the company page
Other documents for Baxter Pharmaceutical Solutions, LLC
  • FDA Inspection 1290838 - 2025-12-11
  • FDA Inspection 1242468 - 2024-09-24
  • FDA Inspection 1243512 - 2024-07-26
  • FDA Inspection 1230675 - 2024-02-20
  • FDA Inspection 1200813 - 2023-02-17

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