Philips North America LLC
FDA inspection history in Bothell, 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 Bothell, Washington.
Cited most
Across all Philips North America observations on file
- 21 CFR 8201
- 21 CFR 820.100Corrective and preventive action1
- 21 CFR 820.198Complaint files1
- 21 CFR 820.75Process validation1
The complete Philips North America file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Bothell, Washington
One Form 483 · 2018 · 4 observations
Latest: Form 483, Dec 3, 2018 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2018-12-03 | 483 Form 483 | Bothell, Washington | 4 | $99 |
Investigators on these documents
FEI number 1000524572 · most recent document Dec 3, 2018
About Philips North America LLC
How many FDA Form 483s has Philips North America LLC received?
FDA Intel has 1 Form 483 on file for Philips North America LLC; the most recent is dated Dec 3, 2018.
When was Philips North America LLC last inspected by FDA?
The most recent FDA inspection document on file for Philips North America LLC is a Form 483 dated Dec 3, 2018, for the site in Bothell, Washington.
What did FDA cite at Philips North America LLC?
The regulations cited most in the observations on file for Philips North America LLC are 21 CFR 820, 1 time; 21 CFR 820.100 (Corrective and preventive action), 1 time; 21 CFR 820.198 (Complaint files), 1 time.