# Candela Corporation – FDA Inspection, Nov 17, 2017

Source: https://www.keypedia.com/records/fda_inspections/candela-corporation/8e00817b-1518-4280-9415-ff2975fd3c75
Source feed: FDA_Inspections

> FDA inspection 1048083 of Candela Corporation, November 17, 2017. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1048083
- Company Name: Candela Corporation
- Inspection Date: 2017-11-17
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: New England District Office
- Citation Count: 0

## Related Documents

- [FDA Inspection 1002942 - 2017-02-08](https://www.keypedia.com/records/fda_inspections/candela-corporation/f5c86fe6-1829-4cdc-8d77-b4d4bc367f1e)
- [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)

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

Office: https://www.keypedia.com/offices/new-england-district-office/aa458072-2f1d-4231-89f5-21ba7a3b7144