Molecular Biologicals, LLC
FDA inspection history in Pasadena, Texas, 2019
- 1
- Form 483
Every document, by year
- Form 483
2019: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at Pasadena, Texas.
Cited most
Across all Molecular Biologicals observations on file
- 21 CFR 803.17What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?1
- 21 CFR 820.198(a)Complaint files1
The complete Molecular Biologicals file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Pasadena, Texas
One Form 483 · 2019 · 2 observations
Latest: Form 483, Sep 26, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-09-26 | 483 Form 483 | Pasadena, Texas | 2 | $99 |
Investigators on these documents
FEI number 3013662224 · most recent document Sep 26, 2019
About Molecular Biologicals, LLC
How many FDA Form 483s has Molecular Biologicals, LLC received?
FDA Intel has 1 Form 483 on file for Molecular Biologicals, LLC; the most recent is dated Sep 26, 2019.
When was Molecular Biologicals, LLC last inspected by FDA?
The most recent FDA inspection document on file for Molecular Biologicals, LLC is a Form 483 dated Sep 26, 2019, for the site in Pasadena, Texas.
What did FDA cite at Molecular Biologicals, LLC?
The regulations cited most in the observations on file for Molecular Biologicals, LLC are 21 CFR 803.17 (What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?), 1 time; 21 CFR 820.198(a) (Complaint files), 1 time.