Allegheny General Hospital
FDA inspection history in Pittsburgh, Pennsylvania, 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 Pittsburgh, Pennsylvania.
Cited most
Across all Allegheny General Hospital observations on file
- 21 CFR 803.17What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?2
- 21 CFR 803.30If I am a user facility, what reporting requirements apply to me?2
- 21 CFR 803.18What are the requirements for establishing and maintaining MDR files or records that apply to me?1
- 21 CFR 803.32If I am a user facility, what information must I submit in my individual adverse event reports?1
The complete Allegheny General Hospital file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Pittsburgh, Pennsylvania
One Form 483 · 2015 · 6 observations
Latest: Form 483, Dec 17, 2015 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2015-12-17 | 483 Form 483 | Pittsburgh, Pennsylvania | 6 | $99 |
Investigators on these documents
FEI number 2521206 · most recent document Dec 17, 2015
About Allegheny General Hospital
How many FDA Form 483s has Allegheny General Hospital received?
FDA Intel has 1 Form 483 on file for Allegheny General Hospital; the most recent is dated Dec 17, 2015.
When was Allegheny General Hospital last inspected by FDA?
The most recent FDA inspection document on file for Allegheny General Hospital is a Form 483 dated Dec 17, 2015, for the site in Pittsburgh, Pennsylvania.
What did FDA cite at Allegheny General Hospital?
The regulations cited most in the observations on file for Allegheny General Hospital are 21 CFR 803.17 (What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?), 2 times; 21 CFR 803.30 (If I am a user facility, what reporting requirements apply to me?), 2 times; 21 CFR 803.18 (What are the requirements for establishing and maintaining MDR files or records that apply to me?), 1 time.