Pushpa Suresh
FDA investigator
Appears on 1 document from 2024, mostly at sites in India. Most often cites general requirements (21 CFR 211.160).
- 1
- Documents on file
- 10.0
- Observations per 483
- 2024
- First seen
- 2024
- Most recent
What they cite most
From 10 observations- 21 CFR 211.160General requirements2
- 21 CFR 211.22Responsibilities of quality control unit2
- 21 CFR 211.67Equipment cleaning and maintenance2
- 21 CFR 211.186Master production and control records1
- 21 CFR 211.188Batch production and control records1
- 21 CFR 211.192Production record review1
Activity by year
2024: 1
Where
India 1
Often inspects with
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Inspection history
1 document, newest first| Date | Firm | Location | Observations | Open |
|---|---|---|---|---|
| 2024-09-27 | 483 Apitoria Pharma Private LimitedSep 27, 2024 · Sangareddy, India | Sangareddy, India | 10 |
About this profile
What does Pushpa Suresh inspect?
Pushpa Suresh appears on 1 document on file covering 1 site, mostly in India.
What do they cite most often?
21 CFR 211.160 (general requirements), followed by 21 CFR 211.22 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 Pushpa Suresh is dated Sep 27, 2024.