# PENTAPHARM AG – FDA Inspection, Sep 15, 2016

Source: https://www.keypedia.com/records/fda_inspections/pentapharm-ag/a6fc0494-430a-4e6d-be89-beab1b7af213
Source feed: FDA_Inspections

> FDA inspection 988595 of PENTAPHARM AG, September 15, 2016. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 988595
- Company Name: PENTAPHARM AG
- Inspection Date: 2016-09-15
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 878383 - 2014-02-20

Company: https://www.keypedia.com/companies/pentapharm-ag/9fe01989-cc6d-4977-b7e7-bdb0071d2207

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