The Feminina Group, Inc.
FDA inspection history in Seattle, Washington, 2018
- 1
- Form 483
Every document, by year
- Form 483
2018: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2018One Form 483, at Seattle, Washington.
Cited most
Across all The Feminina Group observations on file
- 21 CFR 803.17What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?1
- 21 CFR 820.198(a)Complaint files1
The complete The Feminina Group file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Seattle, Washington
One Form 483 · 2018 · 3 observations
Latest: Form 483, Mar 14, 2018 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2018-03-14 | 483 Form 483 | Seattle, Washington | 3 | $99 |
Investigators on these documents
FEI number 3003363230 · most recent document Mar 14, 2018
About The Feminina Group, Inc.
How many FDA Form 483s has The Feminina Group, Inc. received?
FDA Intel has 1 Form 483 on file for The Feminina Group, Inc.; the most recent is dated Mar 14, 2018.
When was The Feminina Group, Inc. last inspected by FDA?
The most recent FDA inspection document on file for The Feminina Group, Inc. is a Form 483 dated Mar 14, 2018, for the site in Seattle, Washington.
What did FDA cite at The Feminina Group, Inc.?
The regulations cited most in the observations on file for The Feminina Group, Inc. are 21 CFR 803.17 (What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?), 1 time; 21 CFR 820.198(a) (Complaint files), 1 time.