Scott E. Norris
FDA investigator
Appears on 3 documents from 2017 to 2019, most often at sites in France. Most often cites production record review (21 CFR 211.192).
- 3
- Documents on file
- 6.7
- Observations per 483
- 2017
- First seen
- 2019
- Most recent
What they cite most
From 20 observations- 21 CFR 211.192Production record review6
- 21 CFR 211.160General requirements2
- 21 CFR 211.68Automatic, mechanical, and electronic equipment2
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.113Control of microbiological contamination1
- 21 CFR 211.166Stability testing1
Activity by year
2017: 1, 2018: 1, 2019: 1
Where
France 1 · Ireland 1 · North Carolina 1
Often inspects with
Anissa M. Cheung· Brentley Collins· Jacqueline Diaz-Albertini
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Inspection history
3 documents, newest first| Date | Firm | Location | Observations | Open |
|---|---|---|---|---|
| 2019-11-26 | 483 Wyeth Pharmaceutical Division of Wyeth Holdings LLCNov 26, 2019 · Sanford, North Carolina | Sanford, North Carolina | 7 | |
| 2018-09-18 | 483 Pfizer Ireland Pharmaceuticals Unlimited CompanySep 18, 2018 · Dublin, Ireland | Dublin, Ireland | 4 | |
| 2017-09-27 | 483 Sanofi Winthrop IndustrieSep 27, 2017 · Marcy L Etoile, France | Marcy L Etoile, France | 9 |
About this profile
What does Scott E. Norris inspect?
Scott E. Norris appears on 3 documents on file covering 3 sites, most often in France.
What do they cite most often?
21 CFR 211.192 (production record review), followed by 21 CFR 211.160 and 21 CFR 211.68.
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 Scott E. Norris is dated Nov 26, 2019.