V. A. Rao
FDA investigator
Appears on 1 document from 2019, mostly at sites in India. Most often cites production record review (21 CFR 211.192).
- 1
- Documents on file
- 4.0
- Observations per 483
- 2019
- First seen
- 2019
- Most recent
What they cite most
From 5 observations- 21 CFR 211.192Production record review2
- 21 CFR 211.188Batch production and control records1
- 21 CFR 211.25Personnel qualifications1
Activity by year
2019: 1
Where
India 1
Often inspects with
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Inspection history
1 document, newest first| Date | Firm | Location | Observations | Open |
|---|---|---|---|---|
| 2019-07-05 | 483 Alivus Life Sciences LimitedJul 5, 2019 · Ankleshwar, India | Ankleshwar, India | 4 |
About this profile
What does V. A. Rao inspect?
V. A. Rao appears on 1 document on file covering 1 site, mostly in India.
What do they cite most often?
21 CFR 211.192 (production record review), followed by 21 CFR 211.188 and 21 CFR 211.25.
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 V. A. Rao is dated Jul 5, 2019.