# FDA Inspection 651048 - Dr. Denise Uetwiller-Geiger - March 04, 2010

Source: https://www.keypedia.com/records/fda_inspections/dr-denise-uetwiller-geiger/aabc0688-2e52-4f8f-ac9e-2b5cd518ded5
Source feed: FDA_Inspections

> FDA Inspection 651048 for Dr. Denise Uetwiller-Geiger on March 04, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 651048
- Company Name: Dr. Denise Uetwiller-Geiger
- Inspection Date: 2010-03-04
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 986899 - 2016-09-13](https://www.keypedia.com/records/fda_inspections/dr-denise-uetwiller-geiger/1363adb5-4d3b-46ba-9ef5-02b8d919f630)

Company: https://www.keypedia.com/companies/dr-denise-uetwiller-geiger/162bca5c-8d08-468b-bcaf-72f7ea12e48b

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