Nortech Laboratories
FDA inspection history in Farmingdale, New York, 2015
- 1
- Form 483
Every document, by year
- Form 483
2015: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2015One Form 483, at Farmingdale, New York.
Cited most
Across all Nortech Laboratories 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 820.198(b)Complaint files1
- 21 CFR 820.72(a)Inspection, measuring, and test equipment1
- 21 CFR 820.75(a)Process validation1
- 21 CFR 820.90(a)Nonconforming product1
The complete Nortech Laboratories file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Farmingdale, New York
One Form 483 · 2015 · 5 observations
Latest: Form 483, Mar 13, 2015 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2015-03-13 | 483 Form 483 | Farmingdale, New York | 5 | $99 |
Investigators on these documents
FEI number 2415591 · most recent document Mar 13, 2015
About Nortech Laboratories
How many FDA Form 483s has Nortech Laboratories received?
FDA Intel has 1 Form 483 on file for Nortech Laboratories; the most recent is dated Mar 13, 2015.
When was Nortech Laboratories last inspected by FDA?
The most recent FDA inspection document on file for Nortech Laboratories is a Form 483 dated Mar 13, 2015, for the site in Farmingdale, New York.
What did FDA cite at Nortech Laboratories?
The regulations cited most in the observations on file for Nortech Laboratories 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 820.198(b) (Complaint files), 1 time; 21 CFR 820.72(a) (Inspection, measuring, and test equipment), 1 time.