Fieldtex Products, Inc
FDA inspection history in Rochester, New York, 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 Rochester, New York.
Cited most
Across all Fieldtex Products observations on file
- 21 CFR 820.100(a)Corrective and preventive action1
- 21 CFR 820.181Device master record1
- 21 CFR 820.184Device history record1
- 21 CFR 820.198(a)Complaint files1
- 21 CFR 820.25(b)Personnel1
The complete Fieldtex Products file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Rochester, New York
One Form 483 · 2022 · 8 observations
Latest: Form 483, Oct 4, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-10-04 | 483 Form 483 | Rochester, New York | 8 | $99 |
Investigators on these documents
FEI number 3000215374 · most recent document Oct 4, 2022
About Fieldtex Products, Inc
How many FDA Form 483s has Fieldtex Products, Inc received?
FDA Intel has 1 Form 483 on file for Fieldtex Products, Inc; the most recent is dated Oct 4, 2022.
When was Fieldtex Products, Inc last inspected by FDA?
The most recent FDA inspection document on file for Fieldtex Products, Inc is a Form 483 dated Oct 4, 2022, for the site in Rochester, New York.
What did FDA cite at Fieldtex Products, Inc?
The regulations cited most in the observations on file for Fieldtex Products, Inc are 21 CFR 820.100(a) (Corrective and preventive action), 1 time; 21 CFR 820.181 (Device master record), 1 time; 21 CFR 820.184 (Device history record), 1 time.