# Squire Boone Caverns, Inc., - Inspection Records

Source: https://www.globalkeysolutions.net/companies/squire-boone-caverns-inc/84718504-6388-43f8-8413-0faaa439dca1

> Inspection records and compliance data for Squire Boone Caverns, Inc., in New Albany, Indiana. Access full analysis and detailed observations.

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## Details

- Name: Squire Boone Caverns, Inc.,
- FEI Number: 1832936
- City: New Albany
- State: Indiana
- Country Name: United States
- Address Line 1: 406 Mount Tabor Rd
- Zip Code: 47150

## Related Documents

- [FDA Inspection 1300382 - Squire Boone Caverns, Inc., - 2026-01-22](https://www.globalkeysolutions.net/records/fda_inspections/squire-boone-caverns-inc/ffbc4025-f74f-4e11-bf7f-8751623dc712) — source: FDA, date: January 22, 2026
- [FDA Inspection 1300382 - Squire Boone Caverns, Inc., - 2026-01-22](https://www.globalkeysolutions.net/records/fda_inspections/squire-boone-caverns-inc/60c77605-1444-4b30-8453-e646db12a5af) — classification: No Action Indicated (NAI), source: FDA, date: January 22, 2026
- [FDA Inspection 1300382 - Squire Boone Caverns, Inc., - 2026-01-22](https://www.globalkeysolutions.net/records/fda_inspections/squire-boone-caverns-inc/3fc0102f-622c-402c-949d-9c85f56358a4) — classification: No Action Indicated (NAI), source: FDA, date: January 22, 2026
- [FDA Inspection 722623 - Squire Boone Caverns, Inc., - 2011-04-21](https://www.globalkeysolutions.net/records/fda_inspections/squire-boone-caverns-inc/b6d950a0-04a8-4f71-9657-f6428046e15f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 21, 2011
- [FDA Inspection 722623 - Squire Boone Caverns, Inc., - 2011-04-21](https://www.globalkeysolutions.net/records/fda_inspections/squire-boone-caverns-inc/3344644b-0026-4b2b-8b7f-79117cb200e7) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 21, 2011
- [FDA Inspection 722623 - Squire Boone Caverns, Inc., - 2011-04-21](https://www.globalkeysolutions.net/records/fda_inspections/squire-boone-caverns-inc/c6c99f4f-b1c2-4185-a146-fd9ba3c2a258) — classification: No Action Indicated (NAI), source: FDA, date: April 21, 2011

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