Myra K. Casey

FDA investigator

Appears on 5 documents from 2002 to 2020, mostly at sites in Indiana. Most often cites postmarketing reporting of adverse drug experiences (21 CFR 314.80(c)(2)).

5
Documents on file
1.0
Observations per 483
2002
First seen
2020
Most recent

What they cite most

From 2 observations

Activity by year

2002: 1, 2008: 1, 2018: 1, 2020: 2

Where

Indiana 4 · Michigan 1

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Inspection history

5 documents, newest first
FirmOpen
EIR Eli Lilly and CompanyMar 20, 2020 · Indianapolis, Indiana
EIR Eli Lilly and CompanyJan 17, 2020 · Indianapolis, Indiana
483 Eli Lilly and CompanyApr 23, 2018 · Indianapolis, Indiana
EIR Depuy Orthopaedics, IncJan 28, 2008 · Warsaw, Indiana
483 Emergent Biodefense Operations Lansing LLCSep 13, 2002 · Lansing, Michigan

About this profile

What does Myra K. Casey inspect?

Myra K. Casey appears on 5 documents on file covering 3 sites, mostly in Indiana.

What do they cite most often?

21 CFR 314.80(c)(2) (postmarketing reporting of adverse drug experiences).

Can I read the observations?

Each document page previews the opening words of every observation. The full documents are available to buy, one at a time or together.

How current is this profile?

The most recent document on file for Myra K. Casey is dated Mar 20, 2020.