Cellpack Ag

Form 483

Villmergen, -, SwitzerlandFEI 3009153862Issued May 01, 2014

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 3009153862.

Observations5

Issue DateMay 01, 2014

StatusNo Warning Letter

Related Inspections3

Establishment Details

Firm: Cellpack Ag
Location: Villmergen, -, Switzerland
FEI Number: 3009153862
Product Type: Devices
Issue Date: May 01, 2014
Country: Switzerland

Inspection History, 2014 to 2026

NAI1

VAI2

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

Act on This Form 483

FDA Inspection ReadinessSee how your operations would hold up to the same scrutiny.CAPA & InvestigationsScore how you would investigate and close findings like these.Talk to a SpecialistWalk through these observations with a ComplianceQuest expert.

Cellpack Ag FDA Form 483, Villmergen, May 1, 2014