# Sofrito El Sembrador - Inspection Records

Source: https://www.globalkeysolutions.net/companies/sofrito-el-sembrador/d37a6282-3909-4830-9392-6cfb78ce5d17

> Inspection records and compliance data for Sofrito El Sembrador in San Sebastian, Puerto Rico. Access full analysis and detailed observations.

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## Details

- Name: Sofrito El Sembrador
- FEI Number: 3003809680
- City: San Sebastian
- State: Puerto Rico
- Country Name: United States
- Address Line 1: Rd 435, Km 2.1 Int. Sector Lizardi, Bo. Calabazas
- Zip Code: 00685

## Related Documents

- [FDA Inspection 1275493 - Sofrito El Sembrador - 2025-07-10](https://www.globalkeysolutions.net/records/fda_inspections/sofrito-el-sembrador/dbec3d4d-a42d-47e8-a59c-70799060f251) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 10, 2025
- [FDA Inspection 1275493 - Sofrito El Sembrador - 2025-07-10](https://www.globalkeysolutions.net/records/fda_inspections/sofrito-el-sembrador/06c46763-921d-49bd-ae65-b97f7f41f23d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 10, 2025
- [FDA Inspection 1275493 - Sofrito El Sembrador - 2025-07-10](https://www.globalkeysolutions.net/records/fda_inspections/sofrito-el-sembrador/900178b8-9022-4a0f-9c83-66e35219525e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 10, 2025
- [FDA Inspection 1080801 - Sofrito El Sembrador - 2019-02-21](https://www.globalkeysolutions.net/records/fda_inspections/sofrito-el-sembrador/e222e5df-b608-4ad1-84dc-8f8ad3553611) — classification: No Action Indicated (NAI), source: FDA, date: February 21, 2019
- [FDA Inspection 965947 - Sofrito El Sembrador - 2016-03-31](https://www.globalkeysolutions.net/records/fda_inspections/sofrito-el-sembrador/b3932599-99f3-4001-a6c3-1bfccb98d40c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 31, 2016
- [FDA Inspection 797925 - Sofrito El Sembrador - 2012-09-07](https://www.globalkeysolutions.net/records/fda_inspections/sofrito-el-sembrador/cb6d58f6-a7d1-40b2-abbe-6b5b9c2969c4) — classification: No Action Indicated (NAI), source: FDA, date: September 7, 2012

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