Twincraft Inc
FDA inspection history in Winooski, Vermont, 2020
- 1
- Form 483
Every document, by year
- Form 483
2020: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2020One Form 483, at Winooski, Vermont.
Cited most
Across all Twincraft observations on file
- 21 CFR 211.194(a)(7)Laboratory records2
- 21 CFR 211.101(a)Charge-in of components1
- 21 CFR 211.113(a)Control of microbiological contamination1
- 21 CFR 211.160(b)(4)General requirements1
- 21 CFR 211.67(a)Equipment cleaning and maintenance1
The complete Twincraft file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Winooski, Vermont
One Form 483 · 2020 · 6 observations
Latest: Form 483, Aug 25, 2020 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2020-08-25 | 483 Form 483 | Winooski, Vermont | 6 | $99 |
Investigators on these documents
FEI number 1219963 · most recent document Aug 25, 2020
About Twincraft Inc
How many FDA Form 483s has Twincraft Inc received?
FDA Intel has 1 Form 483 on file for Twincraft Inc; the most recent is dated Aug 25, 2020.
When was Twincraft Inc last inspected by FDA?
The most recent FDA inspection document on file for Twincraft Inc is a Form 483 dated Aug 25, 2020, for the site in Winooski, Vermont.
What did FDA cite at Twincraft Inc?
The regulations cited most in the observations on file for Twincraft Inc are 21 CFR 211.194(a)(7) (Laboratory records), 2 times; 21 CFR 211.101(a) (Charge-in of components), 1 time; 21 CFR 211.113(a) (Control of microbiological contamination), 1 time.