Asept Pak Inc.

Form 483

Malone, New York, United StatesFEI 3007177643Issued June 20, 2012

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 3007177643.

Observations11

Issue DateJune 20, 2012

StatusNo Warning Letter

Related Inspections7

Establishment Details

Firm: Asept Pak Inc.
Location: Malone, New York, United States
FEI Number: 3007177643
Product Type: Devices
Issue Date: June 20, 2012
Country: United States

Inspection History, 2011 to 2024

NAI1

VAI5

OAI1

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

Asept Pak Inc. FDA Form 483, Malone, New York, June 20, 2012