Stronghaven, Inc. d.b.a Packaging
FDA inspection history in Louisville, Kentucky, 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 Louisville, Kentucky.
Cited most
Across all Stronghaven, Inc. d.b.a Packaging observations on file
- 21 CFR 211.188Batch production and control records1
The complete Stronghaven, Inc. d.b.a Packaging file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Louisville, Kentucky
One Form 483 · 2020 · 1 observation
Latest: Form 483, Feb 21, 2020 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2020-02-21 | 483 Form 483 | Louisville, Kentucky | 1 | $99 |
Investigators on these documents
FEI number 3004903838 · most recent document Feb 21, 2020
About Stronghaven, Inc. d.b.a Packaging
How many FDA Form 483s has Stronghaven, Inc. d.b.a Packaging received?
FDA Intel has 1 Form 483 on file for Stronghaven, Inc. d.b.a Packaging; the most recent is dated Feb 21, 2020.
When was Stronghaven, Inc. d.b.a Packaging last inspected by FDA?
The most recent FDA inspection document on file for Stronghaven, Inc. d.b.a Packaging is a Form 483 dated Feb 21, 2020, for the site in Louisville, Kentucky.
What did FDA cite at Stronghaven, Inc. d.b.a Packaging?
The regulations cited most in the observations on file for Stronghaven, Inc. d.b.a Packaging are 21 CFR 211.188 (Batch production and control records), 1 time.