# FDA Inspection 878550 - Pedicraft, Inc. - April 25, 2014

Source: https://www.keypedia.com/records/fda_inspections/pedicraft-inc/8b5ff560-6c5b-45dd-96e4-a60fc28f9b99
Source feed: FDA_Inspections

> FDA Inspection 878550 for Pedicraft, Inc. on April 25, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 878550
- Company Name: Pedicraft, Inc.
- Inspection Date: 2014-04-25
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: 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