Blendpack, Inc.
FDA inspection history in Cleveland, Tennessee, 2024
- 1
- Form 483
Every document, by year
- Form 483
2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2024One Form 483, at Cleveland, Tennessee.
Cited most
Across all Blendpack observations on file
- 21 CFR 2101
- 21 CFR 211.113(a)Control of microbiological contamination1
- 21 CFR 211.63Equipment design, size, and location1
- 21 CFR 211.84(d)(2)Testing and approval or rejection of components, drug product containers, and closures1
The complete Blendpack file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Cleveland, Tennessee
One Form 483 · 2024 · 4 observations
Latest: Form 483, Nov 1, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-11-01 | 483 Form 483 | Cleveland, Tennessee | 4 | $99 |
FEI number 3013095463 · most recent document Nov 1, 2024
About Blendpack, Inc.
How many FDA Form 483s has Blendpack, Inc. received?
FDA Intel has 1 Form 483 on file for Blendpack, Inc.; the most recent is dated Nov 1, 2024.
When was Blendpack, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Blendpack, Inc. is a Form 483 dated Nov 1, 2024, for the site in Cleveland, Tennessee.
What did FDA cite at Blendpack, Inc.?
The regulations cited most in the observations on file for Blendpack, Inc. are 21 CFR 210, 1 time; 21 CFR 211.113(a) (Control of microbiological contamination), 1 time; 21 CFR 211.63 (Equipment design, size, and location), 1 time.