Medicraft, Inc
FDA inspection history in Elmwood Park, New Jersey, 2024
- 1
- Form 483
Every document, by year
- Form 483
2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2024One Form 483, at Elmwood Park, New Jersey.
Cited most
Across all Medicraft observations on file
- 21 CFR 820.75(a)Process validation2
- 21 CFR 820.100(a)Corrective and preventive action1
- 21 CFR 820.60Identification1
- 21 CFR 820.70(g)(1)Production and process controls1
- 21 CFR 820.72(a)Inspection, measuring, and test equipment1
The complete Medicraft file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Elmwood Park, New Jersey
One Form 483 · 2024 · 7 observations
Latest: Form 483, Nov 27, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-11-27 | 483 Form 483 | Elmwood Park, New Jersey | 7 | $99 |
Investigators on these documents
FEI number 3009538923 · most recent document Nov 27, 2024
About Medicraft, Inc
How many FDA Form 483s has Medicraft, Inc received?
FDA Intel has 1 Form 483 on file for Medicraft, Inc; the most recent is dated Nov 27, 2024.
When was Medicraft, Inc last inspected by FDA?
The most recent FDA inspection document on file for Medicraft, Inc is a Form 483 dated Nov 27, 2024, for the site in Elmwood Park, New Jersey.
What did FDA cite at Medicraft, Inc?
The regulations cited most in the observations on file for Medicraft, Inc are 21 CFR 820.75(a) (Process validation), 2 times; 21 CFR 820.100(a) (Corrective and preventive action), 1 time; 21 CFR 820.60 (Identification), 1 time.