The Belport Company, Inc DBA Gingi-Pak
FDA inspection history in Camarillo, California, 2021
- 1
- Form 483
Every document, by year
- Form 483
2021: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2021One Form 483, at Camarillo, California.
Cited most
Across all The Belport Company, Inc DBA Gingi-Pak observations on file
- 21 CFR 211.100(b)Written procedures; deviations1
- 21 CFR 211.113(a)Control of microbiological contamination1
- 21 CFR 211.130(e)Packaging and labeling operations1
- 21 CFR 211.166(a)Stability testing1
- 21 CFR 211.186(a)Master production and control records1
The complete The Belport Company, Inc DBA Gingi-Pak file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Camarillo, California
One Form 483 · 2021 · 7 observations
Latest: Form 483, Nov 12, 2021 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2021-11-12 | 483 Form 483 | Camarillo, California | 7 | $99 |
Investigators on these documents
FEI number 2014676 · most recent document Nov 12, 2021
About The Belport Company, Inc DBA Gingi-Pak
How many FDA Form 483s has The Belport Company, Inc DBA Gingi-Pak received?
FDA Intel has 1 Form 483 on file for The Belport Company, Inc DBA Gingi-Pak; the most recent is dated Nov 12, 2021.
When was The Belport Company, Inc DBA Gingi-Pak last inspected by FDA?
The most recent FDA inspection document on file for The Belport Company, Inc DBA Gingi-Pak is a Form 483 dated Nov 12, 2021, for the site in Camarillo, California.
What did FDA cite at The Belport Company, Inc DBA Gingi-Pak?
The regulations cited most in the observations on file for The Belport Company, Inc DBA Gingi-Pak are 21 CFR 211.100(b) (Written procedures; deviations), 1 time; 21 CFR 211.113(a) (Control of microbiological contamination), 1 time; 21 CFR 211.130(e) (Packaging and labeling operations), 1 time.