# Candela Corporation – FDA Inspection, Feb 21, 2014

Source: https://www.keypedia.com/records/fda_inspections/candela-corporation/f9438746-42dc-4dd5-9985-641e79449d21
Source feed: FDA_Inspections

> FDA inspection 868362 of Candela Corporation, February 21, 2014. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 803 and 1002. 3 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 868362
- Company Name: Candela Corporation
- Inspection Date: 2014-02-21
- 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: 2

## Related Documents

- [FDA Inspection 1048083 - 2017-11-17](https://www.keypedia.com/records/fda_inspections/candela-corporation/8e00817b-1518-4280-9415-ff2975fd3c75)
- [FDA Inspection 1002942 - 2017-02-08](https://www.keypedia.com/records/fda_inspections/candela-corporation/f5c86fe6-1829-4cdc-8d77-b4d4bc367f1e)
- [FDA Inspection 752274 - 2011-10-18](https://www.keypedia.com/records/fda_inspections/candela-corporation/95a32ff5-99a6-4186-bc5e-e49078bd5854)

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