Kirtida Patel
FDA investigator
Appears on 4 documents from 2008 to 2020, mostly at sites in California. Most often cites complaint files (21 CFR 820.198(a)).
- 4
- Documents on file
- 4.3
- Observations per 483
- 2008
- First seen
- 2020
- Most recent
What they cite most
From 13 observations- 21 CFR 820.198(a)Complaint files4
- 21 CFR 820.100(a)Corrective and preventive action3
- 21 CFR 803.50(a)(1)If I am a manufacturer, what reporting requirements apply to me?1
- 21 CFR 820.186Quality system record1
- 21 CFR 820.22Quality audit1
- 21 CFR 820.30(f)Design controls1
Activity by year
2008: 1, 2013: 1, 2016: 1, 2020: 1
Where
California 4
Often inspects with
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Inspection history
4 documents, newest first| Date | Firm | Location | Observations | Open |
|---|---|---|---|---|
| 2020-10-26 | 483 Medtronic Heart Valves DivisionOct 26, 2020 · Santa Ana, California | Santa Ana, California | 2 | |
| 2016-03-30 | 483 Medtronic Cardiovascular Surgery-theMar 30, 2016 · Santa Ana, California | Santa Ana, California | 2 | |
| 2013-10-03 | 483 Masimo CorporationOct 3, 2013 · Irvine, California | Irvine, California | 9 | |
| 2008-12-01 | EIR Suncoast LaboratoriesDec 1, 2008 · Buena Park, California | Buena Park, California | — |
About this profile
What does Kirtida Patel inspect?
Kirtida Patel appears on 4 documents on file covering 3 sites, mostly in California.
What do they cite most often?
21 CFR 820.198(a) (complaint files), followed by 21 CFR 820.100(a) and 21 CFR 803.50(a)(1).
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 Kirtida Patel is dated Oct 26, 2020.