# Kaiser Permanente Center for Reproductive Health - Inspection Records

Source: https://www.keypedia.com/companies/kaiser-permanente-center-for-reproductive-health/b8e4939a-5e0c-4877-aa93-635fc585b59f

> Inspection records and compliance data for Kaiser Permanente Center for Reproductive Health in Fremont, California. Access full analysis and detailed observations.

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## Details

- Name: Kaiser Permanente Center for Reproductive Health
- FEI Number: 3004740553
- City: Fremont
- State: California
- Country Name: United States
- Address Line 1: 39141 Civic Center Dr Ste 350
- Zip Code: 94538

## Related Documents

- [FDA Inspection 1102672 - Kaiser Permanente Center for Reproductive Health - 2019-09-12](https://www.keypedia.com/records/fda_inspections/kaiser-permanente-center-for-reproductive-health/49d621c9-ee81-47c8-9851-7d663f461841) — classification: No Action Indicated (NAI), source: FDA, date: September 12, 2019
- [FDA Inspection 1102672 - Kaiser Permanente Center for Reproductive Health - 2019-09-12](https://www.keypedia.com/records/fda_inspections/kaiser-permanente-center-for-reproductive-health/b7b2b9ef-51fb-44cb-b123-c31c2cec7969) — classification: No Action Indicated (NAI), source: FDA, date: September 12, 2019
- [FDA Inspection 983869 - Kaiser Permanente Center for Reproductive Health - 2016-08-17](https://www.keypedia.com/records/fda_inspections/kaiser-permanente-center-for-reproductive-health/405b5568-016e-4d8c-97ba-a86d6ba49c33) — classification: No Action Indicated (NAI), source: FDA, date: August 17, 2016
- [FDA Inspection 854836 - Kaiser Permanente Center for Reproductive Health - 2013-10-29](https://www.keypedia.com/records/fda_inspections/kaiser-permanente-center-for-reproductive-health/0a43dde7-3f68-4c68-a079-443c1ba53ed0) — classification: No Action Indicated (NAI), source: FDA, date: October 29, 2013
- [FDA Inspection 751330 - Kaiser Permanente Center for Reproductive Health - 2011-10-26](https://www.keypedia.com/records/fda_inspections/kaiser-permanente-center-for-reproductive-health/9f05fd6d-9753-4f73-a070-6bdcd5338002) — classification: No Action Indicated (NAI), source: FDA, date: October 26, 2011

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