Davol Inc.
FDA inspection history in Warwick, Rhode Island, 2017
- 1
- Form 483
Every document, by year
- Form 483
2017: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2017One Form 483, at Warwick, Rhode Island.
Cited most
Across all Davol observations on file
- 21 CFR 803.50If I am a manufacturer, what reporting requirements apply to me?1
- 21 CFR 820.198Complaint files1
The complete Davol file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Warwick, Rhode Island
One Form 483 · 2017 · 2 observations
Latest: Form 483, Feb 7, 2017 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2017-02-07 | 483 Form 483 | Warwick, Rhode Island | 2 | $99 |
Investigators on these documents
About Davol Inc.
How many FDA Form 483s has Davol Inc. received?
FDA Intel has 1 Form 483 on file for Davol Inc.; the most recent is dated Feb 7, 2017.
When was Davol Inc. last inspected by FDA?
The most recent FDA inspection document on file for Davol Inc. is a Form 483 dated Feb 7, 2017, for the site in Warwick, Rhode Island.
What did FDA cite at Davol Inc.?
The regulations cited most in the observations on file for Davol Inc. are 21 CFR 803.50 (If I am a manufacturer, what reporting requirements apply to me?), 1 time; 21 CFR 820.198 (Complaint files), 1 time.