Chelsea N. Sealey
FDA investigator
Appears on 4 documents from 2015 to 2016, mostly at sites in California. Most often cites general requirements (21 CFR 211.160).
- 4
- Documents on file
- 7.8
- Observations per 483
- 2015
- First seen
- 2016
- Most recent
What they cite most
From 31 observations- 21 CFR 211.160General requirements3
- 21 CFR 211.166Stability testing3
- 21 CFR 211.110Sampling and testing of in-process materials and drug products2
- 21 CFR 211.192Production record review2
- 21 CFR 211.198Complaint files2
- 21 CFR 211.22Responsibilities of quality control unit2
Activity by year
2015: 2, 2016: 2
Where
California 2 · Germany 1 · Puerto Rico 1
Often inspects with
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Inspection history
4 documents, newest first| Date | Firm | Location | Observations | Open |
|---|---|---|---|---|
| 2016-08-18 | 483 World Club Supply CorpAug 18, 2016 · Orange, California | Orange, California | 12 | |
| 2016-03-11 | 483 BSV Bioscience GmbHMar 11, 2016 · Baesweiler, Germany | Baesweiler, Germany | 4 | |
| 2015-06-19 | 483 Pfizer Pharmaceuticals LLCJun 19, 2015 · Vega Baja, Puerto Rico | Vega Baja, Puerto Rico | 5 | |
| 2015-03-06 | 483 Ionia PharmacyMar 6, 2015 · Tustin, California | Tustin, California | 10 |
About this profile
What does Chelsea N. Sealey inspect?
Chelsea N. Sealey appears on 4 documents on file covering 4 sites, mostly in California.
What do they cite most often?
21 CFR 211.160 (general requirements), followed by 21 CFR 211.166 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 Chelsea N. Sealey is dated Aug 18, 2016.