# FDA Inspection 609125 - Helen K. Wu, M.D. - July 22, 2009

Source: https://www.keypedia.com/records/fda_inspections/helen-k-wu-md/98637763-3c49-4a42-a25e-8316127f4a13
Source feed: FDA_Inspections

> FDA Inspection 609125 for Helen K. Wu, M.D. on July 22, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 609125
- Company Name: Helen K. Wu, M.D.
- Inspection Date: 2009-07-22
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 609125 - 2009-07-22](https://www.keypedia.com/records/fda_inspections/helen-k-wu-md/02956233-56ab-4f1d-8cf6-350a0886298a)

Company: https://www.keypedia.com/companies/helen-k-wu-md/4d7d49c3-0eef-4511-9087-da1f64fd6d7c

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