Kathleen R. Jones
FDA investigator
Appears on 4 documents from 2017 to 2021, mostly at sites in Massachusetts. Most often cites production record review (21 CFR 211.192).
- 4
- Documents on file
- 7.3
- Observations per 483
- 2017
- First seen
- 2021
- Most recent
What they cite most
From 22 observations- 21 CFR 211.192Production record review5
- 21 CFR 211.42Design and construction features4
- 21 CFR 211.67Equipment cleaning and maintenance4
- 21 CFR 211.113Control of microbiological contamination2
- 21 CFR 211.160General requirements2
- 21 CFR 211.56Sanitation2
Activity by year
2017: 1, 2020: 1, 2021: 2
Where
Massachusetts 2 · Ireland 1 · New Hampshire 1
Often inspects with
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Inspection history
4 documents, newest first| Date | Firm | Location | Observations | Open |
|---|---|---|---|---|
| 2021-07-23 | 483 Wyeth BioPharma Division of Wyeth Pharmaceuticals LLCJul 23, 2021 · Andover, Massachusetts | Andover, Massachusetts | 13 | |
| 2021-07-23 | EIR Wyeth BioPharma Division of Wyeth Pharmaceuticals LLCJul 23, 2021 · Andover, Massachusetts | Andover, Massachusetts | — | |
| 2020-02-14 | 483 Novo Nordisk US Bio Production Inc.Feb 14, 2020 · West Lebanon, New Hampshire | West Lebanon, New Hampshire | 6 | |
| 2017-05-02 | 483 BioMarin International LimitedMay 2, 2017 · Shanbally, Ireland | Shanbally, Ireland | 3 |
About this profile
What does Kathleen R. Jones inspect?
Kathleen R. Jones appears on 4 documents on file covering 3 sites, mostly in Massachusetts.
What do they cite most often?
21 CFR 211.192 (production record review), followed by 21 CFR 211.42 and 21 CFR 211.67.
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 Kathleen R. Jones is dated Jul 23, 2021.