Satheesh Thomas
FDA investigator
Appears on 3 documents from 2015 to 2018, mostly at sites in India. Most often cites general requirements (21 CFR 211.160).
- 3
- Documents on file
- 4.3
- Observations per 483
- 2015
- First seen
- 2018
- Most recent
What they cite most
From 13 observations- 21 CFR 211.160General requirements3
- 21 CFR 111
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.113Control of microbiological contamination1
- 21 CFR 211.165Testing and release for distribution1
- 21 CFR 211.166Stability testing1
Activity by year
2015: 1, 2017: 1, 2018: 1
Where
India 2 · Netherlands 1
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Inspection history
3 documents, newest first| Date | Firm | Location | Observations | Open |
|---|---|---|---|---|
| 2018-08-28 | 483 Liva Pharmaceuticals LimitedAug 28, 2018 · Vadodara-Halol Highway, India | Vadodara-Halol Highway, India | 1 | |
| 2017-05-05 | 483 Symbiotec Pharmalab Private LimitedMay 5, 2017 · Pithampur, India | Pithampur, India | 6 | |
| 2015-12-11 | 483 Purac Biochem BVDec 11, 2015 · Gorinchem, Netherlands | Gorinchem, Netherlands | 6 |
About this profile
What does Satheesh Thomas inspect?
Satheesh Thomas appears on 3 documents on file covering 3 sites, mostly in India.
What do they cite most often?
21 CFR 211.160 (general requirements), followed by 21 CFR 11 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 Satheesh Thomas is dated Aug 28, 2018.