# Rene B. Allen, M.D., Professional Corporation, Santa Barbara, CA – FDA Inspections

Source: https://www.keypedia.com/companies/rene-b-allen-md-professional-corporation/848ef06c-a6b9-4b68-8211-b3b5d9dad6d3

> Inspection records and compliance data for Rene B. Allen, M.D., Professional Corporation in Santa Barbara, California. 4 FDA inspections on record, last inspected April 02, 2025.

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## Details

- Name: Rene B. Allen, M.D., Professional Corporation
- FEI Number: 3007793483
- Address Line 1: 536 E Arrellaga St Ste 201
- City: Santa Barbara
- State: California
- Zip Code: 93103
- Country Name: United States
- Address: 536 E Arrellaga St Ste 201, Santa Barbara, California 93103, United States
- Country: United States

## Related Documents

- [FDA Inspection 1267236 - Rene B. Allen, M.D., Professional Corporation - 2025-04-02](https://www.keypedia.com/records/fda_inspections/rene-b-allen-md-professional-corporation/74b86490-e184-4ecd-816d-aaa140d14791) — source: FDA, date: April 2, 2025
- FDA Inspection 1267236 - Rene B. Allen, M.D., Professional Corporation - 2025-04-02 — classification: No Action Indicated (NAI), source: FDA, date: April 2, 2025
- FDA Inspection 1267236 - Rene B. Allen, M.D., Professional Corporation - 2025-04-02 — classification: No Action Indicated (NAI), source: FDA, date: April 2, 2025
- FDA Inspection 1096302 - Rene B. Allen, M.D., Professional Corporation - 2019-06-06 — classification: No Action Indicated (NAI), source: FDA, date: June 6, 2019
- FDA Inspection 1096302 - Rene B. Allen, M.D., Professional Corporation - 2019-06-06 — classification: No Action Indicated (NAI), source: FDA, date: June 6, 2019
- [FDA Inspection 974201 - Rene B. Allen, M.D., Professional Corporation - 2016-06-15](https://www.keypedia.com/records/fda_inspections/rene-b-allen-md-professional-corporation/cab0693a-559c-45d1-98b1-ccd8c2b66c50) — classification: No Action Indicated (NAI), source: FDA, date: June 15, 2016
- FDA Inspection 775762 - Rene B. Allen, M.D., Professional Corporation - 2012-04-04 — classification: No Action Indicated (NAI), source: FDA, date: April 4, 2012

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