# FDA Inspection 609807 - Apieron, Inc. - August 28, 2009

Source: https://www.keypedia.com/records/fda_inspections/apieron-inc/633e2bc8-851c-463d-8357-26ec06fca113
Source feed: FDA_Inspections

> FDA Inspection 609807 for Apieron, Inc. on August 28, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 609807
- Company Name: Apieron, Inc.
- Inspection Date: 2009-08-28
- 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 609807 - 2009-08-28](https://www.keypedia.com/records/fda_inspections/apieron-inc/ae5d9dda-544d-4f16-90e9-9dda0170f1ea)

Company: https://www.keypedia.com/companies/apieron-inc/9e49fdec-fe96-4805-9c80-32a8d8c009fa

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