PENTAPHARM AG

Form 483

Aesch Bl, -, SwitzerlandFEI 1000340866Issued September 15, 2016

View FDA's Record for This Firm

Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 1000340866.

Observations1

Issue DateSeptember 15, 2016

StatusNo Warning Letter

Related Inspections2

Establishment Details

Firm: PENTAPHARM AG
Location: Aesch Bl, -, Switzerland
FEI Number: 1000340866
Product Type: Devices
Issue Date: September 15, 2016
Country: Switzerland

Inspection History, 2014 to 2016

NAI1

VAI1

NAI means No Action Indicated. VAI means Voluntary Action Indicated.

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PENTAPHARM AG FDA Form 483, Aesch Bl, September 15, 2016