# Miami Device Solutions, LLC., Miami, FL – FDA Inspections

Source: https://www.keypedia.com/companies/miami-device-solutions-llc/9a61cda8-ed44-4317-9d5c-a2fae34eb83a

> Inspection records and compliance data for Miami Device Solutions, LLC. in Miami, Florida. 4 FDA inspections on record, 1 Form 483, last inspected May 13, 2024.

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## Details

- Name: Miami Device Solutions, LLC.
- FEI Number: 3009222247
- Address Line 1: 7620 Nw 25th St Ste 3
- City: Miami
- State: Florida
- Zip Code: 33122
- Country Name: United States
- Address: 7620 Nw 25th St Ste 3, Miami, Florida 33122, United States
- Country: United States

## Related Documents

- FDA Inspection 1243466 - Miami Device Solutions, LLC. - 2024-05-13 — classification: No Action Indicated (NAI), source: FDA, date: May 13, 2024
- FDA Inspection 1243466 - Miami Device Solutions, LLC. - 2024-05-13 — classification: No Action Indicated (NAI), source: FDA, date: May 13, 2024
- [483 - Miami Device Solutions, LLC. - 2021-09-16](https://www.keypedia.com/records/483/miami-device-solutions-llc/fa68aab0-4f54-4f6d-ba39-46570f72807d) — source: FDA, date: September 16, 2021
- [FDA Inspection 1151858 - Miami Device Solutions, LLC. - 2021-09-16](https://www.keypedia.com/records/fda_inspections/miami-device-solutions-llc/145b7ffc-b1c6-4dee-97ca-fb43163ec2db) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 16, 2021
- FDA Inspection 1106570 - Miami Device Solutions, LLC. - 2019-10-15 — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 15, 2019
- FDA Inspection 1106570 - Miami Device Solutions, LLC. - 2019-10-15 — classification: No Action Indicated (NAI), source: FDA, date: October 15, 2019
- [FDA Inspection 996561 - Miami Device Solutions, LLC. - 2016-10-26](https://www.keypedia.com/records/fda_inspections/miami-device-solutions-llc/3ea099ee-532d-44e2-bcc9-a5825c147831) — classification: No Action Indicated (NAI), source: FDA, date: October 26, 2016
- FDA Inspection 996561 - Miami Device Solutions, LLC. - 2016-10-26 — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 26, 2016

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