Edouard Viard
FDA investigator
Appears on 2 documents from 2016, mostly at sites in New York. Most often cites if I am a manufacturer, what reporting requirements apply to me? (21 CFR 803.50(a)(1)).
- 2
- Documents on file
- 3.0
- Observations per 483
- 2016
- First seen
- 2016
- Most recent
What they cite most
From 6 observations- 21 CFR 803.50(a)(1)If I am a manufacturer, what reporting requirements apply to me?1
- 21 CFR 820.100(b)Corrective and preventive action1
- 21 CFR 820.184Device history record1
- 21 CFR 820.20(e)Management responsibility1
- 21 CFR 820.200(a)Servicing1
- 21 CFR 820.80(e)Receiving, in-process, and finished device acceptance1
Activity by year
2016: 2
Where
New York 2
Often inspects with
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Inspection history
2 documents, newest first| Date | Firm | Location | Observations | Open |
|---|---|---|---|---|
| 2016-06-01 | 483 George Tiemann & CoJun 1, 2016 · Hauppauge, New York | Hauppauge, New York | 1 | |
| 2016-03-01 | 483 Fisher Wallace Laboratories LLCMar 1, 2016 · New York, New York | New York, New York | 5 |
About this profile
What does Edouard Viard inspect?
Edouard Viard appears on 2 documents on file covering 2 sites, mostly in New York.
What do they cite most often?
21 CFR 803.50(a)(1) (if I am a manufacturer, what reporting requirements apply to me?), followed by 21 CFR 820.100(b) and 21 CFR 820.184.
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 Edouard Viard is dated Jun 1, 2016.