# FDA Inspection 992413 - Pedicraft, Inc. - October 19, 2016

Source: https://www.keypedia.com/records/fda_inspections/pedicraft-inc/1c76e912-452a-445b-88a8-6bb7a5082f90
Source feed: FDA_Inspections

> FDA Inspection 992413 for Pedicraft, Inc. on October 19, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 992413
- Company Name: Pedicraft, Inc.
- Inspection Date: 2016-10-19
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/pedicraft-inc/348fce14-ecf0-487a-9b55-1d1d07357e2a

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