# Pacific Reproductive Center - Inspection Records

Source: https://www.globalkeysolutions.net/companies/pacific-reproductive-center/278b5bd8-d3e5-486a-bfad-4eeee6a416fd

> Inspection records and compliance data for Pacific Reproductive Center in Torrance, California. Access full analysis and detailed observations.

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## Details

- Name: Pacific Reproductive Center
- FEI Number: 3005488001
- City: Torrance
- State: California
- Country Name: United States
- Address Line 1: 3720 Lomita Blvd Ste 200
- Zip Code: 90505

## Related Documents

- [483 - Pacific Reproductive Center - 2025-01-13](https://www.globalkeysolutions.net/records/483/pacific-reproductive-center/c1f0e876-4da0-4939-ae9d-93d6f8eec61e) — source: FDA, date: January 13, 2025
- [FDA Inspection 1258255 - Pacific Reproductive Center - 2025-01-13](https://www.globalkeysolutions.net/records/fda_inspections/pacific-reproductive-center/04d8ee8c-443e-43e0-8356-636925a5c9fb) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 13, 2025
- [FDA Inspection 1088043 - Pacific Reproductive Center - 2019-04-02](https://www.globalkeysolutions.net/records/fda_inspections/pacific-reproductive-center/4bf74681-d82a-4459-9759-a01f79459394) — classification: No Action Indicated (NAI), source: FDA, date: April 2, 2019
- [FDA Inspection 1088043 - Pacific Reproductive Center - 2019-04-02](https://www.globalkeysolutions.net/records/fda_inspections/pacific-reproductive-center/9e14626b-149c-41ca-a90a-2bad763cd388) — classification: No Action Indicated (NAI), source: FDA, date: April 2, 2019
- [FDA Inspection 989345 - Pacific Reproductive Center - 2016-08-15](https://www.globalkeysolutions.net/records/fda_inspections/pacific-reproductive-center/b4c5bece-c4c0-4f70-9f66-7abc051cd616) — classification: No Action Indicated (NAI), source: FDA, date: August 15, 2016
- [FDA Inspection 721571 - Pacific Reproductive Center - 2011-04-27](https://www.globalkeysolutions.net/records/fda_inspections/pacific-reproductive-center/26a138ba-8b73-43dd-8d7f-6232c2e2d573) — classification: No Action Indicated (NAI), source: FDA, date: April 27, 2011

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