# HP Hood LLC - Inspection Records

Source: https://www.keypedia.com/companies/hp-hood-llc/3fb2c418-0d6f-48a7-8d14-e208b2694eb5

> Inspection records and compliance data for HP Hood LLC in Philadelphia, Pennsylvania. Access full analysis and detailed observations.

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## Details

- Name: HP Hood LLC
- FEI Number: 2510781
- City: Philadelphia
- State: Pennsylvania
- Country Name: United States
- Address Line 1: 10975 Dutton Rd
- Zip Code: 19154

## Related Documents

- [FDA Inspection 1206597 - HP Hood LLC - 2023-03-09](https://www.keypedia.com/records/fda_inspections/hp-hood-llc/a58784b0-e4a5-4d35-9a04-a4c607ffb12a) — classification: No Action Indicated (NAI), source: FDA, date: March 9, 2023
- [FDA Inspection 1206597 - HP Hood LLC - 2023-03-09](https://www.keypedia.com/records/fda_inspections/hp-hood-llc/14e2c14d-28f1-4155-b378-acfa1cb8aa80) — classification: No Action Indicated (NAI), source: FDA, date: March 9, 2023
- [FDA Inspection 1073228 - HP Hood LLC - 2018-09-19](https://www.keypedia.com/records/fda_inspections/hp-hood-llc/0210be4c-ffd2-4687-a6c1-7dc3e24f2750) — classification: No Action Indicated (NAI), source: FDA, date: September 19, 2018
- [FDA Inspection 1073228 - HP Hood LLC - 2018-09-19](https://www.keypedia.com/records/fda_inspections/hp-hood-llc/8fe1b0c7-8501-487c-8b3b-aee8d0a1cebb) — classification: No Action Indicated (NAI), source: FDA, date: September 19, 2018
- [FDA Inspection 938656 - HP Hood LLC - 2015-08-18](https://www.keypedia.com/records/fda_inspections/hp-hood-llc/621a8a66-8333-41b0-a9de-187aa7d7c6fc) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 18, 2015
- [FDA Inspection 771610 - HP Hood LLC - 2012-02-24](https://www.keypedia.com/records/fda_inspections/hp-hood-llc/684bc465-f94f-45f5-a52f-5d2626668d78) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 24, 2012
- [FDA Inspection 593424 - HP Hood LLC - 2009-06-12](https://www.keypedia.com/records/fda_inspections/hp-hood-llc/f7b11d39-fda4-4726-ac63-c9690402dc00) — classification: No Action Indicated (NAI), source: FDA, date: June 12, 2009

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