Cynthia F. Kleppinger
FDA investigator
Appears on 3 documents from 2013, mostly at sites in Texas. Most often cites investigator recordkeeping and record retention (21 CFR 312.62(a)).
- 3
- Documents on file
- 4.0
- Observations per 483
- 2013
- First seen
- 2013
- Most recent
What they cite most
From 8 observations- 21 CFR 312.62(a)Investigator recordkeeping and record retention2
- 21 CFR 312.53(c)(4)Selecting investigators and monitors1
- 21 CFR 312.56(a)Review of ongoing investigations1
- 21 CFR 312.60General responsibilities of investigators1
- 21 CFR 312.66Assurance of IRB review1
- 21 CFR 50.20General requirements for informed consent1
Activity by year
2013: 3
Where
Texas 2 · Maryland 1
Often inspects with
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Inspection history
3 documents, newest first| Date | Firm | Location | Observations | Open |
|---|---|---|---|---|
| 2013-12-03 | Warning letter Warning letter, Dec 3, 2013Dec 3, 2013 · Houston, Texas | Houston, Texas | — | |
| 2013-03-15 | 483 Stanislaw R Burzynski, M.DMar 15, 2013 · Houston, Maryland | Houston, Maryland | 6 | |
| 2013-03-15 | 483 Burzynski Research InstituteMar 15, 2013 · Houston, Texas | Houston, Texas | 2 |
About this profile
What does Cynthia F. Kleppinger inspect?
Cynthia F. Kleppinger appears on 3 documents on file covering 2 sites, mostly in Texas.
What do they cite most often?
21 CFR 312.62(a) (investigator recordkeeping and record retention), followed by 21 CFR 312.53(c)(4) and 21 CFR 312.56(a).
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 Cynthia F. Kleppinger is dated Dec 3, 2013.