# FDA Inspection 1208125 - Carolon Company - June 15, 2023

Source: https://www.keypedia.com/records/fda_inspections/carolon-company/1bd4acc0-2091-40a5-b820-ef3d69ee1f4e
Source feed: FDA_Inspections

> FDA Inspection 1208125 for Carolon Company on June 15, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1208125
- Company Name: Carolon Company
- Inspection Date: 2023-06-15
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1208125 - 2023-06-15](https://www.keypedia.com/records/fda_inspections/carolon-company/d85cd7bf-f907-4986-9651-8a1104d99d9b)
- [FDA Inspection 988219 - 2016-09-21](https://www.keypedia.com/records/fda_inspections/carolon-company/6dda871a-13a4-4b3f-9f7a-b15ce050d5ad)
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- [FDA Inspection 797456 - 2012-08-06](https://www.keypedia.com/records/fda_inspections/carolon-company/0997cee0-370d-4ee3-8a55-4969740c120e)
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Company: https://www.keypedia.com/companies/carolon-company/0cf14122-8946-4fcc-8af2-b3d7664131f3

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