# Carolon Company – FDA Inspection, Jun 15, 2023

Source: https://www.keypedia.com/records/fda_inspections/carolon-company/d85cd7bf-f907-4986-9651-8a1104d99d9b
Source feed: FDA_Inspections

> FDA inspection 1208125 of Carolon Company, June 15, 2023. Classification: Voluntary Action Indicated (VAI). 7 citations under 21 CFR parts 803 and 820. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1208125
- Company Name: Carolon Company
- Inspection Date: 2023-06-15
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 7

## Related Documents

- FDA Inspection 988219 - 2016-09-21
- FDA Inspection 879287 - 2014-05-08
- [FDA Inspection 797456 - 2012-08-06](https://www.keypedia.com/records/fda_inspections/carolon-company/0997cee0-370d-4ee3-8a55-4969740c120e)
- FDA Inspection 577346 - 2009-04-15

## Related Officers

- [Investigator](https://www.keypedia.com/people/christopher-b-may/b2173a59-d37b-41f1-aa39-eefd854722b8)

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