John A. Sciacchitano
FDA investigator
Appears on 2 documents from 2022 to 2023, mostly at sites in Massachusetts. Most often cites if I am a manufacturer, what information must I submit in my individual adverse event reports? (21 CFR 803.52).
- 2
- Documents on file
- 3.0
- Observations per 483
- 2022
- First seen
- 2023
- Most recent
What they cite most
From 6 observations- 21 CFR 803.52If I am a manufacturer, what information must I submit in my individual adverse event reports?2
- 21 CFR 820.100(a)Corrective and preventive action2
- 21 CFR 820.198(a)Complaint files1
- 21 CFR 820.50(a)(2)Purchasing controls1
Activity by year
2022: 1, 2023: 1
Where
Massachusetts 1 · South Korea 1
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Inspection history
2 documents, newest first| Date | Firm | Location | Observations | Open |
|---|---|---|---|---|
| 2023-09-14 | 483 CELLTRION PHARM, INCSep 14, 2023 · Cheongju, South Korea | Cheongju, South Korea | 3 | |
| 2022-02-16 | 483 Micron Solutions IncFeb 16, 2022 · Fitchburg, Massachusetts | Fitchburg, Massachusetts | 3 |
About this profile
What does John A. Sciacchitano inspect?
John A. Sciacchitano appears on 2 documents on file covering 2 sites, mostly in Massachusetts.
What do they cite most often?
21 CFR 803.52 (if I am a manufacturer, what information must I submit in my individual adverse event reports?), followed by 21 CFR 820.100(a) and 21 CFR 820.198(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 John A. Sciacchitano is dated Sep 14, 2023.