FDA Inspection 850292 - Stille AB - August 22, 2013

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Record Details

This FDA Inspection record concerns Stille AB, with an inspection on August 22, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company: Stille AB
Inspection Date: August 22, 2013
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 4d0d8944-5c73-4419-bc11-e8e4309ca539

Violation Codes6

21 CFR 803.17(b)(2)21 CFR 806.20(b)(4)21 CFR 820.100(a)21 CFR 820.198(a)21 CFR 820.20(c)21 CFR 820.30(e)

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