FDA Inspection
LifeStream Blood BankLifeStream Blood Bank – FDA Inspection, May 14, 2013
Record Details
This FDA Inspection record concerns LifeStream Blood Bank, with an inspection on May 14, 2013, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Company
- LifeStream Blood Bank
- Inspection Date
- May 14, 2013
- Product Type
- Biologics
View Company Profile
ID · 9a087396-a856-4bcc-ad10-9b01dfc01198
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 833540
- FDA center
- Biologics
- Project area
- Blood and Blood Products
FDA Citations
5- 21 CFR 606.100(c)Record review prior to release
- 21 CFR 606.100(c)Thorough investigations
- 21 CFR 606.171Biological product deviation report
- 21 CFR 606.160(a)(1)Concurrent documentation
- 21 CFR 606.100(b)Establish, maintain and follow manufacturing SOPs
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Other FDA inspections of LifeStream Blood Bank
6| Date | Classification | Office | Project area |
|---|---|---|---|
| May 30, 2025 | NAI | Center for Biologics Evaluation and Research | |
| January 13, 2023 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| August 23, 2018 | VAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| November 10, 2015 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| September 29, 2011 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
Other documents for LifeStream Blood Bank
- FDA Inspection 1252910 - 2025-05-30
- FDA Inspection 1195894 - 2023-01-13
- FDA Inspection 1063852 - 2018-08-23
- FDA Inspection 949717 - 2015-11-10
- FDA Inspection 747541 - 2011-09-29
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