Timothy C. Grome
FDA investigator
Appears on 3 documents from 2011 to 2015, mostly at sites in California. Most often cites if I am a manufacturer, what reporting requirements apply to me? (21 CFR 803.50).
- 3
- Documents on file
- 4.0
- Observations per 483
- 2011
- First seen
- 2015
- Most recent
What they cite most
From 4 observations- 21 CFR 803.50If I am a manufacturer, what reporting requirements apply to me?2
- 21 CFR 820.100Corrective and preventive action1
- 21 CFR 820.30Design controls1
Activity by year
2011: 1, 2013: 1, 2015: 1
Where
California 3
Often inspects with
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Inspection history
3 documents, newest first| Date | Firm | Location | Observations | Open |
|---|---|---|---|---|
| 2015-06-30 | EIR Bayer Healthcare LLCJun 30, 2015 · Milpitas, California | Milpitas, California | — | |
| 2013-06-26 | EIR Conceptus, Inc.Jun 26, 2013 · Mountain View, California | Mountain View, California | — | |
| 2011-01-06 | 483 Conceptus, IncJan 6, 2011 · Mountain View, California | Mountain View, California | 4 |
About this profile
What does Timothy C. Grome inspect?
Timothy C. Grome appears on 3 documents on file covering 2 sites, mostly in California.
What do they cite most often?
21 CFR 803.50 (if I am a manufacturer, what reporting requirements apply to me?), followed by 21 CFR 820.100 and 21 CFR 820.30.
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 Timothy C. Grome is dated Jun 30, 2015.