MOOG Medical Devices Group
FDA inspection history in Salt Lake City, Utah, 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 Salt Lake City, Utah.
Cited most
Across all MOOG Medical Devices Group observations on file
- 21 CFR 820.30(f)Design controls3
- 21 CFR 820.100(a)Corrective and preventive action2
- 21 CFR 820.75(a)Process validation2
- 21 CFR 803.50(a)(2)If I am a manufacturer, what reporting requirements apply to me?1
- 21 CFR 820.180General requirements1
The complete MOOG Medical Devices Group file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Salt Lake City, Utah
One Form 483 · 2015 · 15 observations
Latest: Form 483, Jul 30, 2015 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2015-07-30 | 483 Form 483 | Salt Lake City, Utah | 15 | $99 |
Investigators on these documents
FEI number 1000117172 · most recent document Jul 30, 2015
About MOOG Medical Devices Group
How many FDA Form 483s has MOOG Medical Devices Group received?
FDA Intel has 1 Form 483 on file for MOOG Medical Devices Group; the most recent is dated Jul 30, 2015.
When was MOOG Medical Devices Group last inspected by FDA?
The most recent FDA inspection document on file for MOOG Medical Devices Group is a Form 483 dated Jul 30, 2015, for the site in Salt Lake City, Utah.
What did FDA cite at MOOG Medical Devices Group?
The regulations cited most in the observations on file for MOOG Medical Devices Group are 21 CFR 820.30(f) (Design controls), 3 times; 21 CFR 820.100(a) (Corrective and preventive action), 2 times; 21 CFR 820.75(a) (Process validation), 2 times.