Zimmer Manufacturing B.V
FDA inspection history in Mercedita, Puerto Rico, 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 Mercedita, Puerto Rico.
Cited most
Across all Zimmer Manufacturing B.V observations on file
- 21 CFR 820.100(a)Corrective and preventive action1
- 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 Zimmer Manufacturing B.V file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Mercedita, Puerto Rico
One Form 483 · 2015 · 4 observations
Latest: Form 483, Nov 17, 2015 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2015-11-17 | 483 Form 483 | Mercedita, Puerto Rico | 4 | $99 |
Investigators on these documents
Adaliz Santaliz-Cruz (1)Kimberly Lewandowski-Walker (1)Laiza V. Garcia (1)
FEI number 1000132037 · most recent document Nov 17, 2015
About Zimmer Manufacturing B.V
How many FDA Form 483s has Zimmer Manufacturing B.V received?
FDA Intel has 1 Form 483 on file for Zimmer Manufacturing B.V; the most recent is dated Nov 17, 2015.
When was Zimmer Manufacturing B.V last inspected by FDA?
The most recent FDA inspection document on file for Zimmer Manufacturing B.V is a Form 483 dated Nov 17, 2015, for the site in Mercedita, Puerto Rico.
What did FDA cite at Zimmer Manufacturing B.V?
The regulations cited most in the observations on file for Zimmer Manufacturing B.V are 21 CFR 820.100(a) (Corrective and preventive action), 1 time; 21 CFR 820.72(a) (Inspection, measuring, and test equipment), 1 time; 21 CFR 820.75(a) (Process validation), 1 time.