# FDA Inspection 805052 - Fitzco, Inc. - October 29, 2012

Source: https://www.keypedia.com/records/fda_inspections/fitzco-inc/9c48af19-f807-42c6-9b4e-f9b9937bea7a
Source feed: FDA_Inspections

> FDA Inspection 805052 for Fitzco, Inc. on October 29, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 805052
- Company Name: Fitzco, Inc.
- Inspection Date: 2012-10-29
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 994681 - 2016-11-30](https://www.keypedia.com/records/fda_inspections/fitzco-inc/0fc7e0cb-8a4b-430d-9f05-a2e823ad2af1)
- [FDA Inspection 676909 - 2010-08-11](https://www.keypedia.com/records/fda_inspections/fitzco-inc/5b77a604-e20f-4f1b-bf32-3c85a6a82235)

Company: https://www.keypedia.com/companies/fitzco-inc/9e962085-3d4c-4177-a4e4-82e9b7445bbf

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