# New York Blood Center Inc - Inspection Records

Source: https://www.keypedia.com/companies/new-york-blood-center-inc/ffed078a-99a5-4934-961a-8262fee09c76

> Inspection records and compliance data for New York Blood Center Inc in Massapequa, New York. Access full analysis and detailed observations.

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## Details

- Name: New York Blood Center Inc
- FEI Number: 3011940303
- City: Massapequa
- State: New York
- Country Name: United States
- Address Line 1: 1050 Sunrise Hwy
- Zip Code: 11758

## Related Documents

- [483 - New York Blood Center Inc - 2025-12-12](https://www.keypedia.com/records/483/new-york-blood-center-inc/4b525b63-1ad2-44bd-9711-96dfc56e3546) — source: FDA, date: December 12, 2025
- [FDA Inspection 1294968 - New York Blood Center Inc - 2025-12-12](https://www.keypedia.com/records/fda_inspections/new-york-blood-center-inc/3e73ca0b-e8d9-4eeb-8684-afa9b38e4a1e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 12, 2025
- [483 - New York Blood Center Inc - 2021-02-24](https://www.keypedia.com/records/483/new-york-blood-center-inc/46a7dfcb-fdde-4e76-8556-ca7167ebde3a) — source: FDA, date: February 24, 2021
- [FDA Inspection 1136000 - New York Blood Center Inc - 2021-02-24](https://www.keypedia.com/records/fda_inspections/new-york-blood-center-inc/c6a3e9b1-d717-4cb1-85f7-7ec65954c9a1) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 24, 2021
- [483 - New York Blood Center Inc - 2018-05-01](https://www.keypedia.com/records/483/new-york-blood-center-inc/d0dc4e9a-23cc-4a9c-baef-c8ec47f982fe) — source: FDA, date: May 1, 2018
- [FDA Inspection 1050701 - New York Blood Center Inc - 2018-05-01](https://www.keypedia.com/records/fda_inspections/new-york-blood-center-inc/e1a2427e-e077-48ef-805d-9526a5e34b67) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 1, 2018
- [FDA Inspection 969536 - New York Blood Center Inc - 2016-05-06](https://www.keypedia.com/records/fda_inspections/new-york-blood-center-inc/2f6969b0-0920-4c9e-a562-cd22d4647181) — classification: No Action Indicated (NAI), source: FDA, date: May 6, 2016

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