# Productos Mi Gente LLC - Inspection Records

Source: https://www.globalkeysolutions.net/companies/productos-mi-gente-llc/f5b3c16e-fe1b-4371-822f-73b06a7aeb0d

> Inspection records and compliance data for Productos Mi Gente LLC in Mayaguez, Puerto Rico. Access full analysis and detailed observations.

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## Details

- Name: Productos Mi Gente LLC
- FEI Number: 2000026308
- City: Mayaguez
- State: Puerto Rico
- Country Name: United States
- Address Line 1: #101 Calle Dr. Gilberto Concepcion De Gracia
- Zip Code: 00680

## Related Documents

- [FDA Inspection 1051095 - Productos Mi Gente LLC - 2018-05-08](https://www.globalkeysolutions.net/records/fda_inspections/productos-mi-gente-llc/36cbbc13-0954-4933-9ad6-d79050d94508) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 8, 2018
- [FDA Inspection 1051095 - Productos Mi Gente LLC - 2018-05-08](https://www.globalkeysolutions.net/records/fda_inspections/productos-mi-gente-llc/e9396ee5-5055-4e13-911c-b9e5f09330f6) — classification: No Action Indicated (NAI), source: FDA, date: May 8, 2018
- [FDA Inspection 941278 - Productos Mi Gente LLC - 2015-09-15](https://www.globalkeysolutions.net/records/fda_inspections/productos-mi-gente-llc/1337c437-bde4-4ec4-9487-874089c28df3) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 15, 2015
- [FDA Inspection 837371 - Productos Mi Gente LLC - 2013-06-19](https://www.globalkeysolutions.net/records/fda_inspections/productos-mi-gente-llc/b5e15fe9-1d31-411c-9630-237b5b4b4573) — classification: No Action Indicated (NAI), source: FDA, date: June 19, 2013
- [FDA Inspection 837371 - Productos Mi Gente LLC - 2013-06-19](https://www.globalkeysolutions.net/records/fda_inspections/productos-mi-gente-llc/1189f784-9c9a-47a5-abc2-9df2e0a98945) — classification: No Action Indicated (NAI), source: FDA, date: June 19, 2013
- [FDA Inspection 701789 - Productos Mi Gente LLC - 2010-12-10](https://www.globalkeysolutions.net/records/fda_inspections/productos-mi-gente-llc/2db58342-49c1-482b-9cdd-71da1b1cde33) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 10, 2010

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