# Aloe Vera of America, Inc - Inspection Records

Source: https://www.globalkeysolutions.net/companies/aloe-vera-of-america-inc/34db30b2-94e1-4295-a3b3-c067a72f42e9

> Inspection records and compliance data for Aloe Vera of America, Inc in Alton, Texas. Access full analysis and detailed observations.

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## Details

- Name: Aloe Vera of America, Inc
- FEI Number: 1640296
- City: Alton
- State: Texas
- Country Name: United States
- Address Line 1: 1401 S Inspiration Blvd
- Zip Code: 78573

## Related Documents

- [FDA Inspection 1279311 - Aloe Vera of America, Inc - 2025-08-21](https://www.globalkeysolutions.net/records/fda_inspections/aloe-vera-of-america-inc/e919a4ff-8f1b-4bc4-b26b-f41fc14a0cf8) — source: FDA, date: August 21, 2025
- [FDA Inspection 1279311 - Aloe Vera of America, Inc - 2025-08-21](https://www.globalkeysolutions.net/records/fda_inspections/aloe-vera-of-america-inc/43db9b51-aee5-4ea1-bc77-bc64bf93b5ce) — classification: No Action Indicated (NAI), source: FDA, date: August 21, 2025
- [FDA Inspection 1169544 - Aloe Vera of America, Inc - 2022-05-16](https://www.globalkeysolutions.net/records/fda_inspections/aloe-vera-of-america-inc/70ceebd3-5711-40b4-a359-f65b161fd4a9) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 16, 2022
- [FDA Inspection 1069274 - Aloe Vera of America, Inc - 2018-08-02](https://www.globalkeysolutions.net/records/fda_inspections/aloe-vera-of-america-inc/9232ae75-e86f-4ad3-92df-534527ffa738) — classification: No Action Indicated (NAI), source: FDA, date: August 2, 2018
- [FDA Inspection 872931 - Aloe Vera of America, Inc - 2014-01-28](https://www.globalkeysolutions.net/records/fda_inspections/aloe-vera-of-america-inc/125b7204-2642-4d60-ae50-b3a67fd74ed1) — classification: No Action Indicated (NAI), source: FDA, date: January 28, 2014
- [FDA Inspection 652640 - Aloe Vera of America, Inc - 2010-03-18](https://www.globalkeysolutions.net/records/fda_inspections/aloe-vera-of-america-inc/f8973049-578a-4a7e-8900-81f7dc0ed4c9) — classification: No Action Indicated (NAI), source: FDA, date: March 18, 2010

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