PFM Medical Titanium GmbH
FDA inspection history in Nurnberg, Germany, 2016
- 1
- Form 483
Every document, by year
- Form 483
2016: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2016One Form 483, at Nurnberg, Germany.
Cited most
Across all PFM Medical Titanium observations on file
- 21 CFR 820.198Complaint files2
- 21 CFR 803.17What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?1
- 21 CFR 820.100Corrective and preventive action1
- 21 CFR 820.30Design controls1
- 21 CFR 820.50Purchasing controls1
The complete PFM Medical Titanium file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Nurnberg, Germany
One Form 483 · 2016 · 8 observations
Latest: Form 483, Feb 11, 2016 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2016-02-11 | 483 Form 483 | Nurnberg, Germany | 8 | $99 |
Investigators on these documents
FEI number 3003936139 · most recent document Feb 11, 2016
About PFM Medical Titanium GmbH
How many FDA Form 483s has PFM Medical Titanium GmbH received?
FDA Intel has 1 Form 483 on file for PFM Medical Titanium GmbH; the most recent is dated Feb 11, 2016.
When was PFM Medical Titanium GmbH last inspected by FDA?
The most recent FDA inspection document on file for PFM Medical Titanium GmbH is a Form 483 dated Feb 11, 2016, for the site in Nurnberg, Germany.
What did FDA cite at PFM Medical Titanium GmbH?
The regulations cited most in the observations on file for PFM Medical Titanium GmbH are 21 CFR 820.198 (Complaint files), 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 820.100 (Corrective and preventive action), 1 time.