FDA Inspection
Community Blood Center of Greater Kansas City, an Operating Division of New York Blood Center, Inc.Community Blood Center of Greater Kansas City, an Operating Division of New York Blood Center, Inc. – FDA Inspection, Jun 18, 2009
Record Details
This FDA Inspection record concerns Community Blood Center of Greater Kansas City, an Operating Division of New York Blood Center, Inc., with an inspection on June 18, 2009, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Company
- Community Blood Center of Greater Kansas City, an Operating Division of New York Blood Center, Inc.
- Inspection Date
- June 18, 2009
- Product Type
- Biologics
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ID · 93aff5e2-b43b-4ec8-820e-5c8b305515b1
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 592408
- FDA center
- Biologics
- Project area
- Blood and Blood Products
FDA Citations
2- 21 CFR 606.100(c)Thorough investigations
- 21 CFR 606.160(a)(1)Concurrent documentation
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Community Blood Center of Greater Kansas City, an Operating Division of New York Blood Center, Inc.
7| Date | Classification | Office | Project area |
|---|---|---|---|
| March 2, 2026 | Not classified | Kansas City District Office | |
| February 4, 2020 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| March 1, 2018 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| May 16, 2016 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| November 1, 2013 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
Other documents for Community Blood Center of Greater Kansas City, an Operating Division of New York Blood Center, Inc.
- FDA Inspection 1306760 - 2026-03-02
- FDA Inspection 1118733 - 2020-02-04
- FDA Inspection 1044572 - 2018-03-01
- FDA Inspection 970161 - 2016-05-16
- FDA Inspection 853650 - 2013-11-01
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