BioMed Laboratories, LLC
FDA inspection history in Dallas, Texas, 2025
- 1
- Form 483
Every document, by year
- Form 483
2025: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2025One Form 483, at Dallas, Texas.
Cited most
Across all BioMed Laboratories observations on file
- 21 CFR 211.101(d)Charge-in of components1
- 21 CFR 211.160(b)General requirements1
- 21 CFR 211.166(a)Stability testing1
- 21 CFR 211.192Production record review1
- 21 CFR 211.22(d)Responsibilities of quality control unit1
The complete BioMed Laboratories file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Dallas, Texas
One Form 483 · 2025 · 7 observations
Latest: Form 483, Oct 31, 2025 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-10-31 | 483 Form 483 | Dallas, Texas | 7 | $99 |
Investigators on these documents
FEI number 3006784948 · most recent document Oct 31, 2025
About BioMed Laboratories, LLC
How many FDA Form 483s has BioMed Laboratories, LLC received?
FDA Intel has 1 Form 483 on file for BioMed Laboratories, LLC; the most recent is dated Oct 31, 2025.
When was BioMed Laboratories, LLC last inspected by FDA?
The most recent FDA inspection document on file for BioMed Laboratories, LLC is a Form 483 dated Oct 31, 2025, for the site in Dallas, Texas.
What did FDA cite at BioMed Laboratories, LLC?
The regulations cited most in the observations on file for BioMed Laboratories, LLC are 21 CFR 211.101(d) (Charge-in of components), 1 time; 21 CFR 211.160(b) (General requirements), 1 time; 21 CFR 211.166(a) (Stability testing), 1 time.