Buckeye International, Inc.
FDA inspection history in Maryland Heights, Missouri, 2017 to 2021
- 3
- Form 483s
Every document, by year
- Form 483
2017: one Form 483; 2019: one Form 483; 2021: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2017–21Three Form 483s, at Maryland Heights, Missouri.
- 2017The longest 483 on file: 10 observations over 6 pages at Maryland Heights, Missouri.
Cited most
Across all Buckeye International observations on file
- 21 CFR 211.160General requirements2
- 21 CFR 211.198Complaint files2
- 21 CFR 211.22Responsibilities of quality control unit2
- 21 CFR 211.56Sanitation2
- 21 CFR 211.84Testing and approval or rejection of components, drug product containers, and closures2
The complete Buckeye International file.
All 3 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
Maryland Heights, Missouri
Three Form 483s · 2017 to 2021 · 17 observations
Latest: Form 483, Jun 4, 2021 →
Documents
3 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2021-06-04 | 483 Form 483 | Maryland Heights, Missouri | 1 | $99 |
| 2019-06-28 | 483 Form 483 | Maryland Heights, Missouri | 6 | $99 |
| 2017-03-01 | 483 Form 483 | Maryland Heights, Missouri | 10 | $99 |
Investigators on these documents
FEI number 3001419679 · most recent document Jun 4, 2021
About Buckeye International, Inc.
How many FDA Form 483s has Buckeye International, Inc. received?
FDA Intel has 3 Form 483s on file for Buckeye International, Inc.; the most recent is dated Jun 4, 2021.
When was Buckeye International, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Buckeye International, Inc. is a Form 483 dated Jun 4, 2021, for the site in Maryland Heights, Missouri.
What did FDA cite at Buckeye International, Inc.?
The regulations cited most in the observations on file for Buckeye International, Inc. are 21 CFR 211.160 (General requirements), 2 times; 21 CFR 211.198 (Complaint files), 2 times; 21 CFR 211.22 (Responsibilities of quality control unit), 2 times.