Nelson Environmental Technologies, Inc.
FDA inspection history in Stafford, Texas, 2022
- 2
- Form 483s
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 Stafford, Texas.
- 2022The longest 483 on file: 10 observations over 11 pages at Stafford, Texas.
Cited most
Across all Nelson Environmental Technologies observations on file
- 21 CFR 820.100Corrective and preventive action2
- 21 CFR 803.17What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?1
- 21 CFR 820.22Quality audit1
- 21 CFR 820.30(g)Design controls1
- 21 CFR 820.50(b)Purchasing controls1
The complete Nelson Environmental Technologies file.
All 2 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
Stafford, Texas
Two Form 483s · 2022 · 11 observations
Latest: Form 483, Jan 24, 2022 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-01-24 | 483 Form 483 | Stafford, Texas | 10 | $99 |
| Undated | 483 Form 483 | Stafford, Texas | 1 | $99 |
Investigators on these documents
FEI number 3010866895 · most recent document Jan 24, 2022
About Nelson Environmental Technologies, Inc.
How many FDA Form 483s has Nelson Environmental Technologies, Inc. received?
FDA Intel has 2 Form 483s on file for Nelson Environmental Technologies, Inc.; the most recent is dated Jan 24, 2022.
When was Nelson Environmental Technologies, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Nelson Environmental Technologies, Inc. is a Form 483 dated Jan 24, 2022, for the site in Stafford, Texas.
What did FDA cite at Nelson Environmental Technologies, Inc.?
The regulations cited most in the observations on file for Nelson Environmental Technologies, Inc. are 21 CFR 820.100 (Corrective and preventive action), 2 times; 21 CFR 803.17 (What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?), 1 time; 21 CFR 820.22 (Quality audit), 1 time.