# Distributors Ramirez Corp - Inspection Records

Source: https://www.keypedia.com/companies/distributors-ramirez-corp/86dcba1e-4750-4f75-bca3-38537637aa96

> Inspection records and compliance data for Distributors Ramirez Corp in Miami, Florida. Access full analysis and detailed observations.

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## Details

- Name: Distributors Ramirez Corp
- FEI Number: 3004826902
- City: Miami
- State: Florida
- Country Name: United States
- Address Line 1: 1406 NW 23rd St
- Zip Code: 33142

## Related Documents

- [FDA Inspection 865543 - Distributors Ramirez Corp - 2014-02-10](https://www.keypedia.com/records/fda_inspections/distributors-ramirez-corp/9a2cdc66-9c49-4d65-87b2-f72dcbba884b) — classification: No Action Indicated (NAI), source: FDA, date: February 10, 2014
- [FDA Inspection 865543 - Distributors Ramirez Corp - 2014-02-10](https://www.keypedia.com/records/fda_inspections/distributors-ramirez-corp/115915d7-8bb5-439a-b963-0fd8d47fb622) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 10, 2014
- [FDA Inspection 865543 - Distributors Ramirez Corp - 2014-02-10](https://www.keypedia.com/records/fda_inspections/distributors-ramirez-corp/238cb81a-fe1a-4065-a09d-b658093bd6f7) — classification: No Action Indicated (NAI), source: FDA, date: February 10, 2014
- [FDA Inspection 741285 - Distributors Ramirez Corp - 2011-08-22](https://www.keypedia.com/records/fda_inspections/distributors-ramirez-corp/a8e6b470-2258-4750-b3e7-3573a154346d) — classification: No Action Indicated (NAI), source: FDA, date: August 22, 2011
- [FDA Inspection 741285 - Distributors Ramirez Corp - 2011-08-22](https://www.keypedia.com/records/fda_inspections/distributors-ramirez-corp/0a1d8e26-fdd4-4257-8784-3e06b953e05e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 22, 2011
- [FDA Inspection 741285 - Distributors Ramirez Corp - 2011-08-22](https://www.keypedia.com/records/fda_inspections/distributors-ramirez-corp/f9067c1e-8352-4e3b-9bdc-228192bdf700) — classification: No Action Indicated (NAI), source: FDA, date: August 22, 2011

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