Turncare, Inc
FDA inspection history in Pompton Plains, New Jersey, 2023
- 1
- Form 483
Every document, by year
- Form 483
2023: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2023One Form 483, at Pompton Plains, New Jersey.
Cited most
Across all Turncare observations on file
- 21 CFR 803.17(a)(2)What 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 820.184Device history record1
- 21 CFR 820.20(c)Management responsibility1
- 21 CFR 820.22Quality audit1
The complete Turncare file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Pompton Plains, New Jersey
One Form 483 · 2023 · 9 observations
Latest: Form 483, Jun 26, 2023 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-06-26 | 483 Form 483 | Pompton Plains, New Jersey | 9 | $99 |
Investigators on these documents
FEI number 3013682457 · most recent document Jun 26, 2023
About Turncare, Inc
How many FDA Form 483s has Turncare, Inc received?
FDA Intel has 1 Form 483 on file for Turncare, Inc; the most recent is dated Jun 26, 2023.
When was Turncare, Inc last inspected by FDA?
The most recent FDA inspection document on file for Turncare, Inc is a Form 483 dated Jun 26, 2023, for the site in Pompton Plains, New Jersey.
What did FDA cite at Turncare, Inc?
The regulations cited most in the observations on file for Turncare, Inc are 21 CFR 803.17(a)(2) (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 820.184 (Device history record), 1 time.