Reliable Biopharmaceutical, LLC
FDA inspection history in St. Louis, Missouri, 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 St. Louis, Missouri.
Cited most
Across all Reliable Biopharmaceutical observations on file
- 21 CFR 211.68Automatic, mechanical, and electronic equipment2
- 21 CFR 211.160General requirements1
- 21 CFR 211.192Production record review1
- 21 CFR 211.198Complaint files1
- 21 CFR 211.25Personnel qualifications1
The complete Reliable Biopharmaceutical file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
St. Louis, Missouri
One Form 483 · 2020 · 6 observations
Latest: Form 483, Feb 21, 2020 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2020-02-21 | 483 Form 483 | St. Louis, Missouri | 6 | $99 |
Investigators on these documents
FEI number 1927156 · most recent document Feb 21, 2020
About Reliable Biopharmaceutical, LLC
How many FDA Form 483s has Reliable Biopharmaceutical, LLC received?
FDA Intel has 1 Form 483 on file for Reliable Biopharmaceutical, LLC; the most recent is dated Feb 21, 2020.
When was Reliable Biopharmaceutical, LLC last inspected by FDA?
The most recent FDA inspection document on file for Reliable Biopharmaceutical, LLC is a Form 483 dated Feb 21, 2020, for the site in St. Louis, Missouri.
What did FDA cite at Reliable Biopharmaceutical, LLC?
The regulations cited most in the observations on file for Reliable Biopharmaceutical, LLC are 21 CFR 211.68 (Automatic, mechanical, and electronic equipment), 2 times; 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.192 (Production record review), 1 time.