# FDA Inspection 575030 - Aranda Juan, MD - March 26, 2009

Source: https://www.keypedia.com/records/fda_inspections/aranda-juan-md/964fecc3-8892-4a0a-9530-5f65abc1b4e9
Source feed: FDA_Inspections

> FDA Inspection 575030 for Aranda Juan, MD on March 26, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 575030
- Company Name: Aranda Juan, MD
- Inspection Date: 2009-03-26
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 753763 - 2011-11-16](https://www.keypedia.com/records/fda_inspections/aranda-juan-md/6679d138-d485-4ad1-ae0b-8324a8d7bb78)

Company: https://www.keypedia.com/companies/aranda-juan-md/ae33c8b2-856c-4561-a36c-5fda7af46dde

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7