Propak Development, Inc.

Form 483

Dayton, New Jersey, United StatesFEI 3004420929Issued June 17, 2009

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 3004420929.

Observations1

Issue DateJune 17, 2009

StatusNo Warning Letter

Related Inspections2

Establishment Details

Firm: Propak Development, Inc.
Location: Dayton, New Jersey, United States
FEI Number: 3004420929
Product Type: Drugs
Issue Date: June 17, 2009
Country: United States

Inspection History, 2009 to 2013

NAI1

VAI1

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

Act on This Form 483

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Propak Development, Inc. FDA Form 483, Dayton, New Jersey, June 17, 2009