Aditi S. Thakur
FDA investigator
Appears on 4 documents from 2018 to 2024, mostly at sites in India. Most often cites production record review (21 CFR 211.192).
- 4
- Documents on file
- 4.5
- Observations per 483
- 2018
- First seen
- 2024
- Most recent
What they cite most
From 18 observations- 21 CFR 211.192Production record review4
- 21 CFR 211.160General requirements3
- 21 CFR 211.100Written procedures; deviations2
- 21 CFR 211.113Control of microbiological contamination2
- 21 CFR 211.22Responsibilities of quality control unit2
- 21 CFR 211.122Materials examination and usage criteria1
Activity by year
2018: 1, 2020: 1, 2023: 1, 2024: 1
Where
India 2 · South Korea 1 · Spain 1
Often inspects with
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Inspection history
4 documents, newest first| Date | Firm | Location | Observations | Open |
|---|---|---|---|---|
| 2024-06-20 | 483 Binex Co., LtdJun 20, 2024 · Incheon, South Korea | Incheon, South Korea | 4 | |
| 2023-12-07 | 483 Intas Pharmaceuticals LimitedDec 7, 2023 · Ahmedabad, India | Ahmedabad, India | 7 | |
| 2020-01-28 | 483 Dr. Reddy's Laboratories LimitedJan 28, 2020 · Srikakulam District, India | Srikakulam District, India | 4 | |
| 2018-10-16 | 483 Gadea Biopharma $.LOct 16, 2018 · León, Spain | León, Spain | 3 |
About this profile
What does Aditi S. Thakur inspect?
Aditi S. Thakur appears on 4 documents on file covering 4 sites, mostly in India.
What do they cite most often?
21 CFR 211.192 (production record review), followed by 21 CFR 211.160 and 21 CFR 211.100.
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 Aditi S. Thakur is dated Jun 20, 2024.