# FDA Inspection 825133 - Peter Schiff Enterprises - April 12, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/peter-schiff-enterprises/9bf7597e-6c28-4954-8320-19fb55025451
Source feed: FDA_Inspections

> FDA Inspection 825133 for Peter Schiff Enterprises on April 12, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 825133
- Company Name: Peter Schiff Enterprises
- Inspection Date: 2013-04-12
- 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.globalkeysolutions.net/companies/peter-schiff-enterprises/54ddf22d-a5e6-4b03-bafa-efc8fdd59e7e

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