# UCLA Biomedical Cyclotron - Inspection Records

Source: https://www.globalkeysolutions.net/companies/ucla-biomedical-cyclotron/c81bfa21-90ca-4cbb-b13f-8158b4bcaa44

> Inspection records and compliance data for UCLA Biomedical Cyclotron in Los Angeles, California. Access full analysis and detailed observations.

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## Details

- Name: UCLA Biomedical Cyclotron
- FEI Number: 3009211584
- City: Los Angeles
- State: California
- Country Name: United States
- Address Line 1: 780 Westwood Plz
- Zip Code: 90095
- Business Operations: POSITRON EMISSION TOMOGRAPHY DRUG PRODUCTION

## Related Documents

- [483 - UCLA Biomedical Cyclotron - 2025-07-31](https://www.globalkeysolutions.net/records/483/ucla-biomedical-cyclotron/3eb814fe-3b8c-4da9-adfc-f9e4b47ec923) — source: FDA, date: July 31, 2025
- [FDA Inspection 1277145 - UCLA Biomedical Cyclotron - 2025-07-31](https://www.globalkeysolutions.net/records/fda_inspections/ucla-biomedical-cyclotron/83f76beb-b9e2-4a3c-ad10-7606fcb53cc7) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 31, 2025
- [483 - UCLA Biomedical Cyclotron - 2020-07-31](https://www.globalkeysolutions.net/records/483/ucla-biomedical-cyclotron/65378da1-6811-4720-b6c1-047fa7d0879d) — source: FDA, date: July 31, 2020
- [FDA Inspection 1126006 - UCLA Biomedical Cyclotron - 2020-07-31](https://www.globalkeysolutions.net/records/fda_inspections/ucla-biomedical-cyclotron/aaf35993-2f50-487f-a6a8-ef43600362c4) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 31, 2020
- [FDA Inspection 977456 - UCLA Biomedical Cyclotron - 2016-06-02](https://www.globalkeysolutions.net/records/fda_inspections/ucla-biomedical-cyclotron/6771fc8a-ffab-40a2-bdfe-7f1e3ca76775) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 2, 2016
- [FDA Inspection 797880 - UCLA Biomedical Cyclotron - 2012-08-24](https://www.globalkeysolutions.net/records/fda_inspections/ucla-biomedical-cyclotron/24bb03e7-c122-47ec-9e12-2bea2320274b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 24, 2012

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