Urbiel Goldner
FDA investigator
Appears on 1 document from 2009, mostly at sites in Michigan. Most often cites if I am a manufacturer, what reporting requirements apply to me? (21 CFR 803.50(a)(2)).
- 1
- Documents on file
- 7.0
- Observations per 483
- 2009
- First seen
- 2009
- Most recent
What they cite most
From 7 observations- 21 CFR 803.50(a)(2)If I am a manufacturer, what reporting requirements apply to me?1
- 21 CFR 820.198(a)Complaint files1
- 21 CFR 820.25(b)Personnel1
- 21 CFR 820.30(i)Design controls1
- 21 CFR 820.70(b)Production and process controls1
- 21 CFR 820.75(b)Process validation1
Activity by year
2009: 1
Where
Michigan 1
Often inspects with
Charles M. Spyr· Kimberl Lewandowski-Walker· Sullivan Myrick
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Inspection history
1 document, newest first| Date | Firm | Location | Observations | Open |
|---|---|---|---|---|
| 2009-05-15 | 483 Stryker MedicalMay 15, 2009 · Portage, Michigan | Portage, Michigan | 7 |
About this profile
What does Urbiel Goldner inspect?
Urbiel Goldner appears on 1 document on file covering 1 site, mostly in Michigan.
What do they cite most often?
21 CFR 803.50(a)(2) (if I am a manufacturer, what reporting requirements apply to me?), followed by 21 CFR 820.198(a) and 21 CFR 820.25(b).
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 Urbiel Goldner is dated May 15, 2009.