Texas Medical Technology Inc
FDA inspection history in Houston, Texas, 2022
- 1
- Form 483
Every document, by year
- Form 483
2022: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2022One Form 483, at Houston, Texas.
Cited most
Across all Texas Medical Technology 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 820.100(a)Corrective and preventive action1
- 21 CFR 820.120Device labeling1
- 21 CFR 820.181Device master record1
- 21 CFR 820.184Device history record1
The complete Texas Medical Technology file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Houston, Texas
One Form 483 · 2022 · 9 observations
Latest: Form 483, Mar 3, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-03-03 | 483 Form 483 | Houston, Texas | 9 | $99 |
Investigators on these documents
FEI number 3016808907 · most recent document Mar 3, 2022
About Texas Medical Technology Inc
How many FDA Form 483s has Texas Medical Technology Inc received?
FDA Intel has 1 Form 483 on file for Texas Medical Technology Inc; the most recent is dated Mar 3, 2022.
When was Texas Medical Technology Inc last inspected by FDA?
The most recent FDA inspection document on file for Texas Medical Technology Inc is a Form 483 dated Mar 3, 2022, for the site in Houston, Texas.
What did FDA cite at Texas Medical Technology Inc?
The regulations cited most in the observations on file for Texas Medical Technology Inc 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 820.100(a) (Corrective and preventive action), 1 time; 21 CFR 820.120 (Device labeling), 1 time.