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FDA Inspection
•LifeCell Corporation•September 21, 2026

LifeCell Corporation – FDA Inspection, Sep 21, 2026

Record Details

This FDA Inspection record concerns LifeCell Corporation, with an inspection on September 21, 2026, issued by the New Jersey District Office, covering biologics.

Company
LifeCell Corporation
Inspection Date
September 21, 2026
Product Type
Biologics
Office
New Jersey District Office
People
  • Emily A. Walters (Company Rep)
  • Kish Bolden (Issuing Officer)
View Company Profile

ID · 88f4f8d7-7d1a-4e6e-b3c2-96d19d3301db

Inspection Facts

Inspection number
1329332
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 1271.75(d)Donors with risks not determined ineligible

Full citation text and observation details available on the Dashboard.

Other FDA inspections of LifeCell Corporation

12
DateClassificationOfficeProject area
May 21, 2024NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
February 20, 2020NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
June 14, 2019VAICenter for Devices and Radiological HealthCompliance: Devices
January 10, 2019Not classifiedNew Jersey District Office
September 27, 2017NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
View all 12 other inspections on the company page
Other documents for LifeCell Corporation
  • FDA Inspection 1230349 - 2024-05-21
  • FDA Inspection 1120984 - 2020-02-20
  • FDA Inspection 1095091 - 2019-06-14
  • FDA Inspection 1089602 - 2019-01-10
  • FDA Inspection 1028651 - 2017-09-27

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