# Minerva Surgical Incorporated, Santa Clara, CA – FDA Inspections

Source: https://www.keypedia.com/companies/minerva-surgical-incorporated/694add5d-7efb-4206-b7c5-1d7c24389b13

> Inspection records and compliance data for Minerva Surgical Incorporated in Santa Clara, California. 4 FDA inspections on record, last inspected July 14, 2021.

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## Details

- Name: Minerva Surgical Incorporated
- FEI Number: 3011011193
- Address Line 1: 4255 Burton Dr
- City: Santa Clara
- State: California
- Zip Code: 95054
- Country Name: United States
- Address: 4255 Burton Dr, Santa Clara, California 95054, United States
- Country: United States

## Related Documents

- FDA Inspection 1146964 - Minerva Surgical Incorporated - 2021-07-14 — classification: No Action Indicated (NAI), source: FDA, date: July 14, 2021
- FDA Inspection 1146964 - Minerva Surgical Incorporated - 2021-07-14 — classification: No Action Indicated (NAI), source: FDA, date: July 14, 2021
- FDA Inspection 1146964 - Minerva Surgical Incorporated - 2021-07-14 — classification: No Action Indicated (NAI), source: FDA, date: July 14, 2021
- [FDA Inspection 982514 - Minerva Surgical Incorporated - 2016-08-30](https://www.keypedia.com/records/fda_inspections/minerva-surgical-incorporated/aedf1ee0-f44b-46ef-89c8-bec8f21279e6) — classification: No Action Indicated (NAI), source: FDA, date: August 30, 2016
- FDA Inspection 982514 - Minerva Surgical Incorporated - 2016-08-30 — classification: No Action Indicated (NAI), source: FDA, date: August 30, 2016
- FDA Inspection 982514 - Minerva Surgical Incorporated - 2016-08-30 — classification: No Action Indicated (NAI), source: FDA, date: August 30, 2016
- [FDA Inspection 914583 - Minerva Surgical Incorporated - 2015-02-27](https://www.keypedia.com/records/fda_inspections/minerva-surgical-incorporated/23de225d-5efc-4ece-b0eb-705d2c7611ae) — classification: No Action Indicated (NAI), source: FDA, date: February 27, 2015
- FDA Inspection 903446 - Minerva Surgical Incorporated - 2014-11-07 — classification: No Action Indicated (NAI), source: FDA, date: November 7, 2014

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