# Cutera, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/cutera-inc/1e69452e-c590-47af-9b1f-b54e28f2eade

> Inspection records and compliance data for Cutera, Inc. in Brisbane, California. Access full analysis and detailed observations.

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## Details

- Name: Cutera, Inc.
- FEI Number: 3002900199
- City: Brisbane
- State: California
- Country Name: United States
- Address Line 1: 3240 Bayshore Blvd
- Zip Code: 94005

## Related Documents

- [FDA Inspection 1209237 - Cutera, Inc. - 2023-06-26](https://www.keypedia.com/records/fda_inspections/cutera-inc/60877abd-5a08-4fbe-9378-62f6300fad8f) — source: FDA, date: June 26, 2023
- [WARNING_LETTER - Cutera, Inc. - 2023-02-14](https://www.keypedia.com/records/warning_letter/cutera-inc/5056f08f-5512-4401-95fb-3f4e605a510a) — source: FDA, date: February 14, 2023
- [FDA Inspection 1006691 - Cutera, Inc. - 2017-03-15](https://www.keypedia.com/records/fda_inspections/cutera-inc/19328a9f-bcde-4954-a9be-c9acff65d931) — classification: No Action Indicated (NAI), source: FDA, date: March 15, 2017
- [FDA Inspection 1006691 - Cutera, Inc. - 2017-03-15](https://www.keypedia.com/records/fda_inspections/cutera-inc/46c6692d-c1df-4035-b101-35a3f974aacf) — classification: No Action Indicated (NAI), source: FDA, date: March 15, 2017
- [FDA Inspection 983892 - Cutera, Inc. - 2016-08-19](https://www.keypedia.com/records/fda_inspections/cutera-inc/7e19638e-f37c-4dfb-8d73-a073cdb9026a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 19, 2016
- [FDA Inspection 869474 - Cutera, Inc. - 2014-03-25](https://www.keypedia.com/records/fda_inspections/cutera-inc/3dc81993-21b9-4180-a65f-5bb9822e099d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 25, 2014
- [FDA Inspection 869474 - Cutera, Inc. - 2014-03-25](https://www.keypedia.com/records/fda_inspections/cutera-inc/5f2c2bac-0bd7-47f5-a97c-42069e918fa2) — classification: No Action Indicated (NAI), source: FDA, date: March 25, 2014
- [FDA Inspection 806051 - Cutera, Inc. - 2012-11-05](https://www.keypedia.com/records/fda_inspections/cutera-inc/e780ffde-39c1-4869-bdd2-6d99e417c67d) — classification: No Action Indicated (NAI), source: FDA, date: November 5, 2012
- [FDA Inspection 806051 - Cutera, Inc. - 2012-11-05](https://www.keypedia.com/records/fda_inspections/cutera-inc/380c11b9-6c66-4de9-925b-0ee9d61a80d9) — classification: No Action Indicated (NAI), source: FDA, date: November 5, 2012
- [FDA Inspection 806051 - Cutera, Inc. - 2012-11-05](https://www.keypedia.com/records/fda_inspections/cutera-inc/32595dc6-8b63-4fe9-b89c-3c8d99bb2910) — classification: No Action Indicated (NAI), source: FDA, date: November 5, 2012
- [FDA Inspection 742337 - Cutera, Inc. - 2011-08-30](https://www.keypedia.com/records/fda_inspections/cutera-inc/8b0a6fa9-d876-422f-8770-c68a31155142) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 30, 2011

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