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FDA Inspection
•Mckesson Packaging Services•December 15, 2017

Mckesson Packaging Services – FDA Inspection, Dec 15, 2017

Record Details

This FDA Inspection record concerns Mckesson Packaging Services, with an inspection on December 15, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Mckesson Packaging Services
Inspection Date
December 15, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Jared P. Stevens (FDA Associated Person)
  • Susan O. Oladeji (FDA Associated Person)
View Company Profile

ID · 34c2acc9-f679-48aa-94d8-4bc9bd424a35

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1035258
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

FDA Citations

3
  1. 21 CFR 211.160(b)Scientifically sound laboratory controls
  2. 21 CFR 211.186(b)(9)Complete instructions, procedures, specifications et. al.
  3. 21 CFR 211.188(b)(13)Results of drug product inspections and examinations

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Mckesson Packaging Services

4
DateClassificationOfficeProject area
April 22, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 29, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 12, 2011NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 28, 2010NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Mckesson Packaging Services
  • FDA Inspection 969276 - 2016-04-22
  • FDA Inspection 881084 - 2014-05-29
  • FDA Inspection 761612 - 2011-12-12
  • FDA Inspection 645428 - 2010-01-28

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