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FDA Inspection
•Pacon Manufacturing Corporation•April 20, 2016

Pacon Manufacturing Corporation – FDA Inspection, Apr 20, 2016

Record Details

This FDA Inspection record concerns Pacon Manufacturing Corporation, with an inspection on April 20, 2016, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Pacon Manufacturing Corporation
Inspection Date
April 20, 2016
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 7322628c-eccf-41a1-8c13-d160727cd2fe

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
974407
FDA center
Human Drugs
Project area
Drug Quality Assurance

FDA Citations

1
  1. 21 CFR 211.198(a)Complaint Handling Procedure

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Pacon Manufacturing Corporation

4
DateClassificationOfficeProject area
March 13, 2020VAICenter for Devices and Radiological HealthCompliance: Devices
June 20, 2017VAICenter for Devices and Radiological HealthCompliance: Devices
October 24, 2012VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 7, 2010NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Pacon Manufacturing Corporation
  • FDA Inspection 1120832 - 2020-03-13
  • FDA Inspection 1014922 - 2017-06-20
  • FDA Inspection 804886 - 2012-10-24
  • FDA Inspection 637289 - 2010-01-07

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