Anitha P. Govada
FDA investigator
Appears on 1 document from 2019, mostly at sites in India. Most often cites master production and control records (21 CFR 211.186).
- 1
- Documents on file
- 9.0
- Observations per 483
- 2019
- First seen
- 2019
- Most recent
What they cite most
From 9 observations- 21 CFR 211.186Master production and control records2
- 21 CFR 211.192Production record review2
- 21 CFR 211.110Sampling and testing of in-process materials and drug products1
- 21 CFR 211.166Stability testing1
- 21 CFR 211.22Responsibilities of quality control unit1
- 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 |
|---|---|---|---|---|
| 2019-12-20 | 483 ZENARA PHARMA PRIVATE LIMITEDDec 20, 2019 · Hyderabad, India | Hyderabad, India | 9 |
About this profile
What does Anitha P. Govada inspect?
Anitha P. Govada appears on 1 document on file covering 1 site, mostly in India.
What do they cite most often?
21 CFR 211.186 (master production and control records), followed by 21 CFR 211.192 and 21 CFR 211.110.
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 Anitha P. Govada is dated Dec 20, 2019.