# Central California Blood Center - Inspection Records

Source: https://www.keypedia.com/companies/central-california-blood-center/cdb9eb47-661b-4a8c-9976-b9716757419b

> Inspection records and compliance data for Central California Blood Center in Visalia, California. Access full analysis and detailed observations.

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## Details

- Name: Central California Blood Center
- FEI Number: 2970009
- City: Visalia
- State: California
- Country Name: United States
- Address Line 1: 2245 W Caldwell Ave
- Zip Code: 93277

## Related Documents

- [FDA Inspection 1231030 - Central California Blood Center - 2024-02-14](https://www.keypedia.com/records/fda_inspections/central-california-blood-center/213ec249-a2e5-48bf-b42e-edbfa7928262) — classification: No Action Indicated (NAI), source: FDA, date: February 14, 2024
- [FDA Inspection 1086315 - Central California Blood Center - 2019-04-08](https://www.keypedia.com/records/fda_inspections/central-california-blood-center/c2450d46-0a58-4430-82b7-d142b0019cb6) — classification: No Action Indicated (NAI), source: FDA, date: April 8, 2019
- [FDA Inspection 999728 - Central California Blood Center - 2017-01-24](https://www.keypedia.com/records/fda_inspections/central-california-blood-center/0b185f3b-f562-4082-8c0c-2f7ca1a1c151) — classification: No Action Indicated (NAI), source: FDA, date: January 24, 2017
- [FDA Inspection 926973 - Central California Blood Center - 2015-05-18](https://www.keypedia.com/records/fda_inspections/central-california-blood-center/9a2b5306-7814-4a80-a0e6-8611206885e6) — classification: No Action Indicated (NAI), source: FDA, date: May 18, 2015
- [FDA Inspection 829793 - Central California Blood Center - 2013-04-30](https://www.keypedia.com/records/fda_inspections/central-california-blood-center/99e78b82-531b-41e2-9ec6-319d24547b50) — classification: No Action Indicated (NAI), source: FDA, date: April 30, 2013
- [FDA Inspection 728253 - Central California Blood Center - 2011-06-07](https://www.keypedia.com/records/fda_inspections/central-california-blood-center/d329acf1-d22d-4ec4-974c-aca20a0c2ef1) — classification: No Action Indicated (NAI), source: FDA, date: June 7, 2011

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