Ashleigh P. Wodushek
FDA investigator
Appears on 2 documents from 2015, mostly at sites in Colorado. Most often cites corrective and preventive action (21 CFR 820.100(a)).
- 2
- Documents on file
- 8.0
- Observations per 483
- 2015
- First seen
- 2015
- Most recent
What they cite most
From 16 observations- 21 CFR 820.100(a)Corrective and preventive action3
- 21 CFR 820.30(f)Design controls3
- 21 CFR 820.75(a)Process validation2
- 21 CFR 803.50(a)(2)If I am a manufacturer, what reporting requirements apply to me?1
- 21 CFR 820.180General requirements1
- 21 CFR 820.184Device history record1
Activity by year
2015: 2
Where
Colorado 1 · Utah 1
Often inspects with
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Inspection history
2 documents, newest first| Date | Firm | Location | Observations | Open |
|---|---|---|---|---|
| 2015-07-30 | 483 MOOG Medical Devices GroupJul 30, 2015 · Salt Lake City, Utah | Salt Lake City, Utah | 15 | |
| 2015-05-22 | 483 Cardinal Health 200 IncMay 22, 2015 · Denver, Colorado | Denver, Colorado | 1 |
About this profile
What does Ashleigh P. Wodushek inspect?
Ashleigh P. Wodushek appears on 2 documents on file covering 2 sites, mostly in Colorado.
What do they cite most often?
21 CFR 820.100(a) (corrective and preventive action), followed by 21 CFR 820.30(f) and 21 CFR 820.75(a).
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 Ashleigh P. Wodushek is dated Jul 30, 2015.