FDA Inspection
LifeSource-Upper Midwest OPOLifeSource-Upper Midwest OPO – FDA Inspection, Jan 24, 2012
Record Details
This FDA Inspection record concerns LifeSource-Upper Midwest OPO, with an inspection on January 24, 2012, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Company
- LifeSource-Upper Midwest OPO
- Inspection Date
- January 24, 2012
- Product Type
- Biologics
View Company Profile
ID · 4b6a0a3e-0caa-4355-a42b-2dcfa7e8c5a7
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 758993
- FDA center
- Biologics
- Project area
- Human Cellular, Tissue, and Gene Therapies
FDA Citations
3- 21 CFR 1271.160(a)All core requirements covered in program
- 21 CFR 1271.180(a)Procedures to meet core CTGP
- 21 CFR 1271.270(a)Accurate, indelible, legible
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Other FDA inspections of LifeSource-Upper Midwest OPO
6| Date | Classification | Office | Project area |
|---|---|---|---|
| July 30, 2025 | Not classified | Minneapolis District Office | |
| March 22, 2019 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| September 20, 2017 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| February 9, 2015 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| October 24, 2012 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
Other documents for LifeSource-Upper Midwest OPO
- FDA Inspection 1279132 - 2025-07-30
- FDA Inspection 1084827 - 2019-03-22
- FDA Inspection 1028803 - 2017-09-20
- FDA Inspection 913084 - 2015-02-09
- FDA Inspection 805924 - 2012-10-24
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