# 8617 Northern Blvd Corp - Inspection Records

Source: https://www.keypedia.com/companies/8617-northern-blvd-corp/62754937-9584-4218-8f4e-8d7123c28193

> Inspection records and compliance data for 8617 Northern Blvd Corp in Woodside, New York. Access full analysis and detailed observations.

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## Details

- Name: 8617 Northern Blvd Corp
- FEI Number: 3004334030
- City: Woodside
- State: New York
- Country Name: United States
- Address Line 1: 3049 60th St
- Zip Code: 11377

## Related Documents

- [FDA Inspection 1222139 - 8617 Northern Blvd Corp - 2023-11-07](https://www.keypedia.com/records/fda_inspections/8617-northern-blvd-corp/9dc71674-c8f8-424c-8592-a87015cb4cf7) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 7, 2023
- [FDA Inspection 1199434 - 8617 Northern Blvd Corp - 2023-03-09](https://www.keypedia.com/records/fda_inspections/8617-northern-blvd-corp/4532c01c-7acd-405f-ae50-552eda793e84) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 9, 2023
- [FDA Inspection 940601 - 8617 Northern Blvd Corp - 2015-08-19](https://www.keypedia.com/records/fda_inspections/8617-northern-blvd-corp/82b25257-5679-45b5-90da-a192079822e1) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 19, 2015
- [FDA Inspection 775094 - 8617 Northern Blvd Corp - 2012-03-22](https://www.keypedia.com/records/fda_inspections/8617-northern-blvd-corp/22612012-e684-4fc3-b460-493a86dffcc6) — classification: Official Action Indicated (OAI), source: FDA, date: March 22, 2012
- [FDA Inspection 720505 - 8617 Northern Blvd Corp - 2011-04-26](https://www.keypedia.com/records/fda_inspections/8617-northern-blvd-corp/e990f694-e7cb-4958-b211-133b3cbc6426) — classification: Official Action Indicated (OAI), source: FDA, date: April 26, 2011
- [FDA Inspection 674582 - 8617 Northern Blvd Corp - 2010-08-03](https://www.keypedia.com/records/fda_inspections/8617-northern-blvd-corp/36db4b11-42d7-48ef-bd19-e1eaa972143c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 3, 2010

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