# Candela Corporation – FDA Inspection, Feb 8, 2017

Source: https://www.keypedia.com/records/fda_inspections/candela-corporation/f5c86fe6-1829-4cdc-8d77-b4d4bc367f1e
Source feed: FDA_Inspections

> FDA inspection 1002942 of Candela Corporation, February 08, 2017. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 803 and 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1002942
- Company Name: Candela Corporation
- Inspection Date: 2017-02-08
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- [FDA Inspection 1048083 - 2017-11-17](https://www.keypedia.com/records/fda_inspections/candela-corporation/8e00817b-1518-4280-9415-ff2975fd3c75)
- [FDA Inspection 868362 - 2014-02-21](https://www.keypedia.com/records/fda_inspections/candela-corporation/f9438746-42dc-4dd5-9985-641e79449d21)
- [FDA Inspection 752274 - 2011-10-18](https://www.keypedia.com/records/fda_inspections/candela-corporation/95a32ff5-99a6-4186-bc5e-e49078bd5854)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/james-p-finn/70e5c36c-2711-449b-bf73-e08b4dd58449)
- [FDA Associated Person](https://www.keypedia.com/people/stephen-c-smith/426649fa-0e5b-4b35-ba41-636512a06a48)

Company: https://www.keypedia.com/companies/candela-corporation/17da0021-1ef2-48bf-b786-70bd590e80b5

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