Stephanie D. Crockett
FDA investigator
Appears on 3 documents from 2016, mostly at sites in Florida. Most often cites general requirements (21 CFR 211.160).
- 3
- Documents on file
- 9.0
- Observations per 483
- 2016
- First seen
- 2016
- Most recent
What they cite most
From 27 observations- 21 CFR 211.160General requirements3
- 21 CFR 211.192Production record review3
- 21 CFR 211.194Laboratory records3
- 21 CFR 211.100Written procedures; deviations2
- 21 CFR 211.165Testing and release for distribution2
- 21 CFR 211.42(c)(10)(iv)Design and construction features2
Activity by year
2016: 3
Where
Florida 3
Often inspects with
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Inspection history
3 documents, newest first| Date | Firm | Location | Observations | Open |
|---|---|---|---|---|
| 2016-07-28 | 483 Hybrid Pharma LLCJul 28, 2016 · Deerfield Beach, Florida | Deerfield Beach, Florida | 9 | |
| 2016-05-13 | 483 Belcher Pharmaceuticals, LLCMay 13, 2016 · Largo, Florida | Largo, Florida | 9 | |
| 2016-01-15 | 483 Actavis Laboratories, FL, IncJan 15, 2016 · Davie, Florida | Davie, Florida | 9 |
About this profile
What does Stephanie D. Crockett inspect?
Stephanie D. Crockett appears on 3 documents on file covering 3 sites, mostly in Florida.
What do they cite most often?
21 CFR 211.160 (general requirements), followed by 21 CFR 211.192 and 21 CFR 211.194.
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 Stephanie D. Crockett is dated Jul 28, 2016.