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FDA Inspection
•Catalent Pharma Solutions LLC•May 24, 2024

Catalent Pharma Solutions LLC – FDA Inspection, May 24, 2024

Record Details

This FDA Inspection record concerns Catalent Pharma Solutions LLC, with an inspection on May 24, 2024, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Catalent Pharma Solutions LLC
Inspection Date
May 24, 2024
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
People
  • Richard L. Bartlett (Issuing Officer)
  • Travis S. Bradley (FDA Associated Person)
View Company Profile

ID · 94f7b472-03a3-4b38-89b4-0e7c1214c26e

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1229061
FDA center
Biologics
Project area
Blood and Blood Products

FDA Citations

1
  1. 21 CFR 211.67(a)Cleaning / Sanitizing / Maintenance

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Catalent Pharma Solutions LLC

12
DateClassificationOfficeProject area
May 22, 2026Not classifiedAtlanta District OfficeDrug Quality Assurance
December 15, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 28, 2020OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 20, 2019NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 2, 2019Not classifiedAtlanta District Office
View all 12 other inspections on the company page
Other documents for Catalent Pharma Solutions LLC
  • FDA Inspection 1303072 - 2026-05-22
  • FDA Inspection 1195585 - 2022-12-15
  • FDA Inspection 1131607 - 2020-09-28
  • FDA Inspection 1116748 - 2019-12-20
  • FDA Inspection 1102199 - 2019-08-02

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Contact
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