Turbo Wheelchair Co. Inc.
FDA inspection history in Louisville, Kentucky, 2017
- 1
- Form 483
Every document, by year
- Form 483
2017: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2017One Form 483, at Louisville, Kentucky.
Cited most
Across all Turbo Wheelchair Co. 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 820.181Device master record1
- 21 CFR 820.184Device history record1
- 21 CFR 820.20(e)Management responsibility1
The complete Turbo Wheelchair Co. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Louisville, Kentucky
One Form 483 · 2017 · 10 observations
Latest: Form 483, May 2, 2017 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2017-05-02 | 483 Form 483 | Louisville, Kentucky | 10 | $99 |
Investigators on these documents
FEI number 3004149089 · most recent document May 2, 2017
About Turbo Wheelchair Co. Inc.
How many FDA Form 483s has Turbo Wheelchair Co. Inc. received?
FDA Intel has 1 Form 483 on file for Turbo Wheelchair Co. Inc.; the most recent is dated May 2, 2017.
When was Turbo Wheelchair Co. Inc. last inspected by FDA?
The most recent FDA inspection document on file for Turbo Wheelchair Co. Inc. is a Form 483 dated May 2, 2017, for the site in Louisville, Kentucky.
What did FDA cite at Turbo Wheelchair Co. Inc.?
The regulations cited most in the observations on file for Turbo Wheelchair Co. 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 820.181 (Device master record), 1 time.