# Skeletal Dynamics, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/skeletal-dynamics-inc/01c75cc2-64c2-4b6f-9923-d6f13c178f71

> Inspection records and compliance data for Skeletal Dynamics, Inc. in Miami, Florida. 4 FDA inspections on record, last inspected April 05, 2024.

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## Details

- Name: Skeletal Dynamics, Inc.
- FEI Number: 3006742481
- Address Line 1: 7300 N Kendall Dr Ste 800
- City: Miami
- State: Florida
- Zip Code: 33156
- Country Name: United States
- Address: 7300 N Kendall Dr Ste 800, Miami, Florida 33156, United States
- Country: United States

## Related Documents

- FDA Inspection 1235650 - Skeletal Dynamics, Inc. - 2024-04-05 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 5, 2024
- [FDA Inspection 1235650 - Skeletal Dynamics, Inc. - 2024-04-05](https://www.keypedia.com/records/fda_inspections/skeletal-dynamics-inc/ec764944-084f-489c-b4a7-881ced10ac00) — classification: No Action Indicated (NAI), source: FDA, date: April 5, 2024
- [483 - Skeletal Dynamics, Inc. - 2022-02-18](https://www.keypedia.com/records/483/skeletal-dynamics-inc/fa735a8e-1635-41ec-83e1-51ccab407d43) — source: FDA, date: February 18, 2022
- FDA Inspection 1162542 - Skeletal Dynamics, Inc. - 2022-02-18 — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 18, 2022
- FDA Inspection 1162542 - Skeletal Dynamics, Inc. - 2022-02-18 — classification: No Action Indicated (NAI), source: FDA, date: February 18, 2022
- FDA Inspection 938043 - Skeletal Dynamics, Inc. - 2015-07-29 — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 29, 2015
- FDA Inspection 938043 - Skeletal Dynamics, Inc. - 2015-07-29 — classification: No Action Indicated (NAI), source: FDA, date: July 29, 2015
- FDA Inspection 895894 - Skeletal Dynamics, Inc. - 2014-09-15 — classification: No Action Indicated (NAI), source: FDA, date: September 15, 2014
- FDA Inspection 895894 - Skeletal Dynamics, Inc. - 2014-09-15 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 15, 2014

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