# Sarati International, Inc, Los Fresnos, TX – FDA Inspections

Source: https://www.keypedia.com/companies/sarati-international-inc/046eadcd-3abf-4486-8b64-5d7ec464ac9d

> Inspection records and compliance data for Sarati International, Inc in Los Fresnos, Texas. 6 FDA inspections on record, 2 Form 483s, last inspected March 21, 2025.

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## Details

- Name: Sarati International, Inc
- FEI Number: 3002979812
- Address Line 1: 27502 Ted Hunt Rd
- City: Los Fresnos
- State: Texas
- Zip Code: 78566
- Country Name: United States
- Address: 27502 Ted Hunt Rd, Los Fresnos, Texas 78566, United States
- Country: United States

## Related Documents

- FDA Inspection 1256177 - Sarati International, Inc - 2025-03-21 — source: FDA, date: March 21, 2025
- [FDA Inspection 1256177 - Sarati International, Inc - 2025-03-21](https://www.keypedia.com/records/fda_inspections/sarati-international-inc/62f6f22d-f711-4adc-bd2a-1db31bf4ea97) — classification: No Action Indicated (NAI), source: FDA, date: March 21, 2025
- [FDA Inspection 1093755 - Sarati International, Inc - 2019-06-13](https://www.keypedia.com/records/fda_inspections/sarati-international-inc/175183c5-2d9e-4048-8153-76bf5ec7ac9c) — source: FDA, date: June 13, 2019
- [FDA Inspection 1021815 - Sarati International, Inc - 2017-06-30](https://www.keypedia.com/records/fda_inspections/sarati-international-inc/e6791cbf-3eba-4e42-b11e-130cc4131540) — source: FDA, date: June 30, 2017
- FDA Inspection 953924 - Sarati International, Inc - 2015-11-20 — classification: No Action Indicated (NAI), source: FDA, date: November 20, 2015
- FDA Inspection 732571 - Sarati International, Inc - 2011-06-29 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 29, 2011
- [FDA Inspection 732571 - Sarati International, Inc - 2011-06-29](https://www.keypedia.com/records/fda_inspections/sarati-international-inc/f8113aaa-f78e-4797-8483-93e9a798c74e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 29, 2011
- FDA Inspection 613028 - Sarati International, Inc - 2009-08-31 — classification: No Action Indicated (NAI), source: FDA, date: August 31, 2009

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