# FDA Inspection 938043 - Skeletal Dynamics, Inc. - July 29, 2015

Source: https://www.keypedia.com/records/fda_inspections/skeletal-dynamics-inc/afff1152-9905-4791-ab28-9e5fe3b01488
Source feed: FDA_Inspections

> FDA inspection 938043 of Skeletal Dynamics, Inc., July 29, 2015. Classification: No Action Indicated (NAI). 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 938043
- Company Name: Skeletal Dynamics, Inc.
- Inspection Date: 2015-07-29
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1235650 - 2024-04-05](https://www.keypedia.com/records/fda_inspections/skeletal-dynamics-inc/ec764944-084f-489c-b4a7-881ced10ac00)
- FDA Inspection 1162542 - 2022-02-18
- FDA Inspection 895894 - 2014-09-15

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

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7