FDA Inspection
LifeCell CorporationLifeCell Corporation – FDA Inspection, Jan 10, 2019
Record Details
This FDA Inspection record concerns LifeCell Corporation, with an inspection on January 10, 2019, issued by the New Jersey District Office, covering medical devices & rad health.
- Company
- LifeCell Corporation
- Inspection Date
- January 10, 2019
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · fb559597-19ce-42e5-86ae-79a0ab93f936
Inspection Facts
- Inspection number
- 1089602
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of LifeCell Corporation
12| Date | Classification | Office | Project area |
|---|---|---|---|
| September 21, 2026 | Not classified | New Jersey District Office | Human Cellular, Tissue, and Gene Therapies |
| May 21, 2024 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| February 20, 2020 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| June 14, 2019 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 27, 2017 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
Other documents for LifeCell Corporation
- FDA Inspection 1329332 - 2026-09-21
- FDA Inspection 1230349 - 2024-05-21
- FDA Inspection 1120984 - 2020-02-20
- FDA Inspection 1095091 - 2019-06-14
- FDA Inspection 1028651 - 2017-09-27
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