Lindsey Brown
FDA investigator · also recorded as Ee Lindsey Brown
Appears on 4 documents from 2017 to 2024, most often at sites in Belgium. Most often cites general requirements (21 CFR 211.160).
- 4
- Documents on file
- 6.0
- Observations per 483
- 2017
- First seen
- 2024
- Most recent
What they cite most
From 24 observations- 21 CFR 211.160General requirements5
- 21 CFR 211.100Written procedures; deviations4
- 21 CFR 211.113Control of microbiological contamination2
- 21 CFR 211.186Master production and control records2
- 21 CFR 211.192Production record review2
- 21 CFR 211.22Responsibilities of quality control unit2
Activity by year
2017: 1, 2021: 1, 2023: 1, 2024: 1
Where
Belgium 1 · Denmark 1 · India 1 · Texas 1
Often inspects with
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Inspection history
4 documents, newest first| Date | Firm | Location | Observations | Open |
|---|---|---|---|---|
| 2024-03-25 | 483 Novo Nordisk A/SMar 25, 2024 · Kalundborg, Denmark | Kalundborg, Denmark | 8 | |
| 2023-06-07 | 483 FUJIFILM Diosynth Biotechnologies Texas, LLCJun 7, 2023 · College Station, Texas | College Station, Texas | 8 | |
| 2021-10-26 | 483 Catalent Belgium S.AOct 26, 2021 · Brussels, Belgium | Brussels, Belgium | 7 | |
| 2017-04-07 | 483 Biocon LimitedApr 7, 2017 · Bangalore, India | Bangalore, India | 1 |
About this profile
What does Lindsey Brown inspect?
Lindsey Brown appears on 4 documents on file covering 4 sites, most often in Belgium.
What do they cite most often?
21 CFR 211.160 (general requirements), followed by 21 CFR 211.100 and 21 CFR 211.113.
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 Lindsey Brown is dated Mar 25, 2024.