McKesson Corporation
Form 483 issued July 3, 2018 · San Francisco, Washington
- Inspection
- Jun 25 – Jul 3, 2018
- Investigator
- Jolanna A. Norton
- Observations
- 3
- Pages
- 3
- FEI number
- 3014548060
In short: On July 3, 2018, FDA issued a Form 483 with 3 observations to McKesson Corporation in San Francisco, Washington (FEI 3014548060) after an inspection that ran Jun 25 – Jul 3, 2018. The investigator was Jolanna A. Norton.
What FDA observed
Preview: the opening words of each observation- 01
The systems in place to enable compliance with the requirements of the Food Drug and Cosmetic…
- 02
Failure to make a determination regarding product subject to an illegitimate product notification…
- 03
Systems and procedures to make notifications following determination of an illegitimate product are deficient in that…
This inspection in context
Jolanna A. Norton
22 documents · 2017–2026
Cites FDCA 501(a)(2)(A) (insanitary conditions) more than any other section. Most of their documents are for sites in California.
The firmMcKesson Corporation history
All 2 documents on file for this site, in date order, with what was cited at each inspection.
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Questions about this 483
What did FDA find at McKesson Corporation?
FDA listed 3 observations on this Form 483. The opening words of each observation are shown on this page.
Who inspected McKesson Corporation?
Jolanna A. Norton is named on this Form 483, for the inspection of Jun 25 – Jul 3, 2018. Each investigator has a profile showing what they cite most.
When was McKesson Corporation inspected by FDA?
The inspection ran Jun 25 – Jul 3, 2018, and the Form 483 is dated July 3, 2018.
How do I get the full Form 483 for McKesson Corporation?
Download the original PDF from FDA Intel for $99, with no subscription. Your first Form 483 or letter is on us. You also get an invoice PDF with the order.