FDA Inspection
Cutera, Inc.Cutera, Inc. – FDA Inspection, Jan 12, 2018
Record Details
This FDA Inspection record concerns Cutera, Inc., with an inspection on January 12, 2018, issued by the San Francisco District Office, covering medical devices & rad health.
- Company
- Cutera, Inc.
- Inspection Date
- January 12, 2018
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · 5f24acad-77df-4284-8885-0863eb015be6
Inspection Facts
- Inspection number
- 1052101
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Cutera, Inc.
6| Date | Classification | Office | Project area |
|---|---|---|---|
| June 26, 2023 | Not classified | San Francisco District Office | |
| March 15, 2017 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| August 19, 2016 | VAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| March 25, 2014 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| November 5, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Cutera, Inc.
- FDA Inspection 1209237 - 2023-06-26
- FDA Inspection 1006691 - 2017-03-15
- FDA Inspection 983892 - 2016-08-19
- FDA Inspection 869474 - 2014-03-25
- FDA Inspection 806051 - 2012-11-05
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