Physic-Control, Inc
FDA inspection history in Redmond, Washington, 2017 to 2019
- 2
- Form 483s
Every document, by year
- Form 483
2017: one Form 483; 2019: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2017–19Two Form 483s, at Redmond, Washington.
- 2019The longest 483 on file: 5 observations over 4 pages at Redmond, Washington.
Cited most
Across all Physic-Control observations on file
- 21 CFR 820.100(a)Corrective and preventive action2
- 21 CFR 803.52(b)(2)If I am a manufacturer, what information must I submit in my individual adverse event reports?1
- 21 CFR 803.56If I am a manufacturer, in what circumstances must I submit a supplemental or followup report and what are the requirements for such reports?1
- 21 CFR 820.30(f)Design controls1
- 21 CFR 820.50(a)(1)Purchasing controls1
The complete Physic-Control file.
All 2 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
Redmond, Washington
Two Form 483s · 2017 to 2019 · 7 observations
Latest: Form 483, Nov 26, 2019 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-11-26 | 483 Form 483 | Redmond, Washington | 5 | $99 |
| 2017-12-15 | 483 Form 483 | Redmond, Washington | 2 | $99 |
Investigators on these documents
FEI number 3015876 · most recent document Nov 26, 2019
About Physic-Control, Inc
How many FDA Form 483s has Physic-Control, Inc received?
FDA Intel has 2 Form 483s on file for Physic-Control, Inc; the most recent is dated Nov 26, 2019.
When was Physic-Control, Inc last inspected by FDA?
The most recent FDA inspection document on file for Physic-Control, Inc is a Form 483 dated Nov 26, 2019, for the site in Redmond, Washington.
What did FDA cite at Physic-Control, Inc?
The regulations cited most in the observations on file for Physic-Control, Inc are 21 CFR 820.100(a) (Corrective and preventive action), 2 times; 21 CFR 803.52(b)(2) (If I am a manufacturer, what information must I submit in my individual adverse event reports?), 1 time; 21 CFR 803.56 (If I am a manufacturer, in what circumstances must I submit a supplemental or followup report and what are the requirements for such reports?), 1 time.